rs28937895

Orientation

plus

Stabilized

plus

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

Make rs28937895(A;A)

Make rs28937895(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6302287

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs28937895
dbSNP (classic)	rs28937895
ClinGen	rs28937895
ebi	rs28937895
HLI	rs28937895
Exac	rs28937895
Gnomad	rs28937895
Varsome	rs28937895
LitVar	rs28937895
Map	rs28937895
PheGenI	rs28937895
Biobank	rs28937895
1000 genomes	rs28937895
hgdp	rs28937895
ensembl	rs28937895
geneview	rs28937895
scholar	rs28937895
google	rs28937895
pharmgkb	rs28937895
gwascentral	rs28937895
openSNP	rs28937895
23andMe	rs28937895
SNPshot	rs28937895
SNPdbe	rs28937895
MSV3d	rs28937895
GWAS Ctlg	rs28937895

Max Magnitude

0

deafness

OMIM	606201
Desc	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 6
Variant	0017
Related	also

ClinVar
Risk	rs28937895(A;A) rs28937895(C;C)
Alt	rs28937895(A;A) rs28937895(C;C)
Reference	Rs28937895(G;G)
Significance	Pathogenic
Disease	WFS1-Related Disorders
Variation	info
Gene	WFS1
CLNDBN	WFS1-Related Disorders
Reversed	0
HGVS	NC_000004.11:g.6304014G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004781.3,