rs71524377

Orientation

plus

Stabilized

plus

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

Make rs71524377(A;A)

Make rs71524377(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6301914

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs71524377
dbSNP (classic)	rs71524377
ClinGen	rs71524377
ebi	rs71524377
HLI	rs71524377
Exac	rs71524377
Gnomad	rs71524377
Varsome	rs71524377
LitVar	rs71524377
Map	rs71524377
PheGenI	rs71524377
Biobank	rs71524377
1000 genomes	rs71524377
hgdp	rs71524377
ensembl	rs71524377
geneview	rs71524377
scholar	rs71524377
google	rs71524377
pharmgkb	rs71524377
gwascentral	rs71524377
openSNP	rs71524377
23andMe	rs71524377
SNPshot	rs71524377
SNPdbe	rs71524377
MSV3d	rs71524377
GWAS Ctlg	rs71524377

Max Magnitude

0

ClinVar
Risk	rs71524377(A;A) rs71524377(T;T)
Alt	rs71524377(A;A) rs71524377(T;T)
Reference	Rs71524377(G;G)
Significance	Pathogenic
Disease	not specified Diabetes mellitus AND insipidus with optic atrophy AND deafness
Variation	info
Gene	WFS1
CLNDBN	not specified Diabetes mellitus AND insipidus with optic atrophy AND deafness
Reversed	0
HGVS	NC_000004.11:g.6303641G>A; NC_000004.11:g.6303641G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000200753.2, RCV000023510.4,