12 | g.5968959T>A | CA13752541 | VWF | c.7729+252A>T (n.7729+252A>T)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.5968959T>C | CA2581068293 | VWF | c.7729+252A>G (n.7729+252A>G)
| |
12 | g.5968959T>G | CA2581068294 | VWF | c.7729+252A>C (n.7729+252A>C)
| |
12 | g.5968959T= | CA2013849778 | VWF | c.7729+252A= (n.7729+252A=)
| |
12 | g.5968965G>A | CA690484006 | VWF | c.7729+246C>T (n.7729+246C>T)
| dbSNP |
12 | g.5968965G= | CA2013849779 | VWF | c.7729+246C= (n.7729+246C=)
| |
12 | g.5968965G>T | CA2794405279 | VWF | c.7729+246C>A (n.7729+246C>A)
| |
12 | g.5968968G>A | CA2013849781 | VWF | c.7729+243C>T (n.7729+243C>T)
| dbSNP |
12 | g.5968968G= | CA2013849780 | VWF | c.7729+243C= (n.7729+243C=)
| |
12 | g.5968969T>C | CA232281520 | VWF | c.7729+242A>G (n.7729+242A>G)
| dbSNP |
12 | g.5968969T= | CA2013849782 | VWF | c.7729+242A= (n.7729+242A=)
| |
12 | g.5968972C= | CA2013849784 | VWF | c.7729+239G= (n.7729+239G=)
| |
12 | g.5968972C>G | CA944315212 | VWF | c.7729+239G>C (n.7729+239G>C)
| dbSNP gnomAD v3 gnomAD v4 |
12 | g.5968972C>T | CA2013849783 | VWF | c.7729+239G>A (n.7729+239G>A)
| dbSNP |
12 | g.5968984A= | CA2013849785 | VWF | c.7729+227T= (n.7729+227T=)
| |
12 | g.5968984A>C | CA232281528 | VWF | c.7729+227T>G (n.7729+227T>G)
| dbSNP |
12 | g.5968986C= | CA2013849786 | VWF | c.7729+225G= (n.7729+225G=)
| |
12 | g.5968986C>G | CA232281536 | VWF | c.7729+225G>C (n.7729+225G>C)
| dbSNP gnomAD v3 gnomAD v4 |
12 | g.5968990G>A | CA232281554 | VWF | c.7729+221C>T (n.7729+221C>T)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.5968990G>C | CA2013849788 | VWF | c.7729+221C>G (n.7729+221C>G)
| dbSNP |
12 | g.5968990G= | CA2013849787 | VWF | c.7729+221C= (n.7729+221C=)
| |
12 | g.5968991G>A | CA2013849790 | VWF | c.7729+220C>T (n.7729+220C>T)
| dbSNP |
12 | g.5968991G= | CA2013849789 | VWF | c.7729+220C= (n.7729+220C=)
| |
12 | g.5968992G>A | CA944315231 | VWF | c.7729+219C>T (n.7729+219C>T)
| dbSNP gnomAD v3 gnomAD v4 |
12 | g.5968992G= | CA2013849791 | VWF | c.7729+219C= (n.7729+219C=)
| |
12 | g.5968994C= | CA2013849792 | VWF | c.7729+217G= (n.7729+217G=)
| |
12 | g.5968994C>T | CA603090384 | VWF | c.7729+217G>A (n.7729+217G>A)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.5968995G>A | CA232281574 | VWF | c.7729+216C>T (n.7729+216C>T)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.5968995G= | CA2013849793 | VWF | c.7729+216C= (n.7729+216C=)
| |
12 | g.5969000C>A | CA944315237 | VWF | c.7729+211G>T (n.7729+211G>T)
| dbSNP gnomAD v3 gnomAD v4 |
12 | g.5969000C= | CA2013849794 | VWF | c.7729+211G= (n.7729+211G=)
| |
12 | g.5969001C= | CA2013849796 | VWF | c.7729+210G= (n.7729+210G=)
| |
12 | g.5969001C>T | CA2013849797 | VWF | c.7729+210G>A (n.7729+210G>A)
| dbSNP |
12 | g.5969001_5969014delinsCAGTCTTGCCATGT | CA2013849795 | VWF | c.7729+197_7729+210delinsACATGGCAAGACTG (n.7729+197_7729+210delinsACATGGCAAGACTG)
| |
12 | g.5969002A= | CA2013849798 | VWF | c.7729+209T= (n.7729+209T=)
| |
12 | g.5969002A>C | CA690484026 | VWF | c.7729+209T>G (n.7729+209T>G)
| dbSNP gnomAD v3 gnomAD v4 |
12 | g.5969002A>G | CA690484019 | VWF | c.7729+209T>C (n.7729+209T>C)
| dbSNP gnomAD v3 gnomAD v4 |
12 | g.5969005_5969017del | CA690484041 | VWF | c.7729+197_7729+209del (n.7729+197_7729+209del)
| dbSNP |
12 | g.5969006T>A | CA232281584 | VWF | c.7729+205A>T (n.7729+205A>T)
| dbSNP gnomAD v3 gnomAD v4 |
12 | g.5969006T= | CA2013849799 | VWF | c.7729+205A= (n.7729+205A=)
| |
12 | g.5969008G>C | CA2013849801 | VWF | c.7729+203C>G (n.7729+203C>G)
| dbSNP gnomAD v3 |
12 | g.5969008G= | CA2013849800 | VWF | c.7729+203C= (n.7729+203C=)
| |
12 | g.5969012T>C | CA2013849803 | VWF | c.7729+199A>G (n.7729+199A>G)
| dbSNP |
12 | g.5969012T= | CA2013849802 | VWF | c.7729+199A= (n.7729+199A=)
| |
12 | g.5969013G>A | CA690484047 | VWF | c.7729+198C>T (n.7729+198C>T)
| dbSNP gnomAD v3 gnomAD v4 |
12 | g.5969013G= | CA2013849804 | VWF | c.7729+198C= (n.7729+198C=)
| |
12 | g.5969015A= | CA2013849805 | VWF | c.7729+196T= (n.7729+196T=)
| |
12 | g.5969015A>T | CA2013849806 | VWF | c.7729+196T>A (n.7729+196T>A)
| dbSNP |
12 | g.5969016G>C | CA603090387 | VWF | c.7729+195C>G (n.7729+195C>G)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.5969016G= | CA2013849807 | VWF | c.7729+195C= (n.7729+195C=)
| |