rs1800378

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs1800378(A;G)

Make rs1800378(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

6063036

Gene

VWF

is a	snp
is	mentioned by
dbSNP	rs1800378
dbSNP (classic)	rs1800378
ClinGen	rs1800378
ebi	rs1800378
HLI	rs1800378
Exac	rs1800378
Gnomad	rs1800378
Varsome	rs1800378
LitVar	rs1800378
Map	rs1800378
PheGenI	rs1800378
Biobank	rs1800378
1000 genomes	rs1800378
hgdp	rs1800378
ensembl	rs1800378
geneview	rs1800378
scholar	rs1800378
google	rs1800378
pharmgkb	rs1800378
gwascentral	rs1800378
openSNP	rs1800378
23andMe	rs1800378
SNPshot	rs1800378
SNPdbe	rs1800378
MSV3d	rs1800378
GWAS Ctlg	rs1800378

GMAF

0.4775

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs1800378(G;G) rs1800378(T;T)
Alt	rs1800378(G;G) rs1800378(T;T)
Reference	Rs1800378(A;A)
Significance	Probable-non-pathogenic
Disease	not specified von Willebrand disorder
Variation	info
Gene	VWF
CLNDBN	not specified von Willebrand disorder
Reversed	1
HGVS	NC_000012.11:g.6172202T>C
CLNSRC
CLNACC	RCV000249735.1, RCV000390452.1,