rs28934879

Merged into

rs121964895

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0

Make rs28934879(A;A)

Make rs28934879(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

6021960

Gene

VWF

is a	snp
is	mentioned by
dbSNP	rs28934879
dbSNP (classic)	rs28934879
ClinGen	rs28934879
ebi	rs28934879
HLI	rs28934879
Exac	rs28934879
Gnomad	rs28934879
Varsome	rs28934879
LitVar	rs28934879
Map	rs28934879
PheGenI	rs28934879
Biobank	rs28934879
1000 genomes	rs28934879
hgdp	rs28934879
ensembl	rs28934879
geneview	rs28934879
scholar	rs28934879
google	rs28934879
pharmgkb	rs28934879
gwascentral	rs28934879
openSNP	rs28934879
23andMe	rs28934879
SNPshot	rs28934879
SNPdbe	rs28934879
MSV3d	rs28934879
GWAS Ctlg	rs28934879

Status

Merged into rs121964895

Max Magnitude

0

OMIM	193400
Desc	VON WILLEBRAND DISEASE, TYPE IIM
Variant	0027
Related	also