rs1801208

Orientation

plus

Stabilized

plus

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

Make rs1801208(A;A)

Make rs1801208(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6301162

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs1801208
dbSNP (classic)	rs1801208
ClinGen	rs1801208
ebi	rs1801208
HLI	rs1801208
Exac	rs1801208
Gnomad	rs1801208
Varsome	rs1801208
LitVar	rs1801208
Map	rs1801208
PheGenI	rs1801208
Biobank	rs1801208
1000 genomes	rs1801208
hgdp	rs1801208
ensembl	rs1801208
geneview	rs1801208
scholar	rs1801208
google	rs1801208
pharmgkb	rs1801208
gwascentral	rs1801208
openSNP	rs1801208
23andMe	rs1801208
SNPshot	rs1801208
SNPdbe	rs1801208
MSV3d	rs1801208
GWAS Ctlg	rs1801208

GMAF

0.05556

Max Magnitude

0

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

[PMID 19258739] Association study of the effect of WFS1 polymorphisms on risk of type 2 diabetes in Japanese population

ClinVar
Risk	rs1801208(A;A)
Alt	rs1801208(A;A)
Reference	Rs1801208(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Nonsyndromic Hearing Loss WFS1-Related Spectrum Disorders
Variation	info
Gene	WFS1
CLNDBN	not specified Nonsyndromic Hearing Loss, Dominant WFS1-Related Spectrum Disorders
Reversed	0
HGVS	NC_000004.11:g.6302889G>A
CLNSRC	HGMD UniProtKB (protein)
CLNACC	RCV000038638.8, RCV000269758.1, RCV000363867.1,