rs369107336

Orientation

plus

Stabilized

plus

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

Make rs369107336(C;G)

Make rs369107336(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

6302164

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs369107336
dbSNP (classic)	rs369107336
ClinGen	rs369107336
ebi	rs369107336
HLI	rs369107336
Exac	rs369107336
Gnomad	rs369107336
Varsome	rs369107336
LitVar	rs369107336
Map	rs369107336
PheGenI	rs369107336
Biobank	rs369107336
1000 genomes	rs369107336
hgdp	rs369107336
ensembl	rs369107336
geneview	rs369107336
scholar	rs369107336
google	rs369107336
pharmgkb	rs369107336
gwascentral	rs369107336
openSNP	rs369107336
23andMe	rs369107336
SNPshot	rs369107336
SNPdbe	rs369107336
MSV3d	rs369107336
GWAS Ctlg	rs369107336

Max Magnitude

0

ClinVar
Risk	rs369107336(A;A) rs369107336(G;G) rs369107336(T;T)
Alt	rs369107336(A;A) rs369107336(G;G) rs369107336(T;T)
Reference	Rs369107336(C;C)
Significance	Pathogenic
Disease	Wolfram syndrome not specified
Variation	info
Gene	WFS1
CLNDBN	Wolfram syndrome not specified
Reversed	0
HGVS	NC_000004.11:g.6303891C>A; NC_000004.11:g.6303891C>G; NC_000004.11:g.6303891C>T
CLNSRC
CLNACC	RCV000193050.1, RCV000152697.3, RCV000218719.1,