rs1800382

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs1800382(A;A)

Make rs1800382(A;G)

Reference

GRCh38 38.1/142

Chromosome

12

Position

6019222

Gene

VWF

is a	snp
is	mentioned by
dbSNP	rs1800382
dbSNP (classic)	rs1800382
ClinGen	rs1800382
ebi	rs1800382
HLI	rs1800382
Exac	rs1800382
Gnomad	rs1800382
Varsome	rs1800382
LitVar	rs1800382
Map	rs1800382
PheGenI	rs1800382
Biobank	rs1800382
1000 genomes	rs1800382
hgdp	rs1800382
ensembl	rs1800382
geneview	rs1800382
scholar	rs1800382
google	rs1800382
pharmgkb	rs1800382
gwascentral	rs1800382
openSNP	rs1800382
23andMe	rs1800382
SNPshot	rs1800382
SNPdbe	rs1800382
MSV3d	rs1800382
GWAS Ctlg	rs1800382

Max Magnitude

0

OMIM	613160
Desc
Variant	0010
Related	also

ClinVar
Risk	rs1800382(A;A)
Alt	rs1800382(A;A)
Reference	Rs1800382(G;G)
Significance	Non-pathogenic
Disease	VON WILLEBRAND FACTOR POLYMORPHISM
Variation	info
Gene	VWF
CLNDBN	VON WILLEBRAND FACTOR POLYMORPHISM
Reversed	1
HGVS	NC_000012.11:g.6128388C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000000317.2,