rs876657675

Orientation

plus

Stabilized

plus

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

Make rs876657675(C;C)

Make rs876657675(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

4

Position

6302303

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs876657675
dbSNP (classic)	rs876657675
ClinGen	rs876657675
ebi	rs876657675
HLI	rs876657675
Exac	rs876657675
Gnomad	rs876657675
Varsome	rs876657675
LitVar	rs876657675
Map	rs876657675
PheGenI	rs876657675
Biobank	rs876657675
1000 genomes	rs876657675
hgdp	rs876657675
ensembl	rs876657675
geneview	rs876657675
scholar	rs876657675
google	rs876657675
pharmgkb	rs876657675
gwascentral	rs876657675
openSNP	rs876657675
23andMe	rs876657675
SNPshot	rs876657675
SNPdbe	rs876657675
MSV3d	rs876657675
GWAS Ctlg	rs876657675

Max Magnitude

0

ClinVar
Risk	rs876657675(C;C)
Alt	rs876657675(C;C)
Reference	Rs876657675(G;G)
Significance	Probable-Pathogenic
Disease	WFS1-Related Disorders
Variation	info
Gene	WFS1
CLNDBN	WFS1-Related Disorders
Reversed	0
HGVS	NC_000004.11:g.6304030G>C
CLNSRC
CLNACC	RCV000219504.1,