rs104893882

Orientation

plus

Stabilized

plus

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

Make rs104893882(A;C)

Make rs104893882(C;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6301696

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs104893882
dbSNP (classic)	rs104893882
ClinGen	rs104893882
ebi	rs104893882
HLI	rs104893882
Exac	rs104893882
Gnomad	rs104893882
Varsome	rs104893882
LitVar	rs104893882
Map	rs104893882
PheGenI	rs104893882
Biobank	rs104893882
1000 genomes	rs104893882
hgdp	rs104893882
ensembl	rs104893882
geneview	rs104893882
scholar	rs104893882
google	rs104893882
pharmgkb	rs104893882
gwascentral	rs104893882
openSNP	rs104893882
23andMe	rs104893882
SNPshot	rs104893882
SNPdbe	rs104893882
MSV3d	rs104893882
GWAS Ctlg	rs104893882

Max Magnitude

0

OMIM	606201
Desc
Variant	0018
Related	also

ClinVar
Risk	rs104893882(C;C) rs104893882(G;G)
Alt	rs104893882(C;C) rs104893882(G;G)
Reference	Rs104893882(A;A)
Significance	Pathogenic
Disease	WFS1-Related Disorders
Variation	info
Gene	WFS1
CLNDBN	WFS1-Related Disorders
Reversed	0
HGVS	NC_000004.11:g.6303423A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004782.3,