rs28937894

Orientation

plus

Stabilized

plus

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

Make rs28937894(C;T)

Make rs28937894(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6301891

Gene

WFS1

is a	snp
is	mentioned by
dbSNP	rs28937894
dbSNP (classic)	rs28937894
ClinGen	rs28937894
ebi	rs28937894
HLI	rs28937894
Exac	rs28937894
Gnomad	rs28937894
Varsome	rs28937894
LitVar	rs28937894
Map	rs28937894
PheGenI	rs28937894
Biobank	rs28937894
1000 genomes	rs28937894
hgdp	rs28937894
ensembl	rs28937894
geneview	rs28937894
scholar	rs28937894
google	rs28937894
pharmgkb	rs28937894
gwascentral	rs28937894
openSNP	rs28937894
23andMe	rs28937894
SNPshot	rs28937894
SNPdbe	rs28937894
MSV3d	rs28937894
GWAS Ctlg	rs28937894

Max Magnitude

0

deafness

OMIM	606201
Desc	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 6
Variant	0016
Related	also

ClinVar
Risk	rs28937894(T;T)
Alt	rs28937894(T;T)
Reference	Rs28937894(C;C)
Significance	Pathogenic
Disease	WFS1-Related Disorders not specified
Variation	info
Gene	WFS1
CLNDBN	WFS1-Related Disorders not specified
Reversed	0
HGVS	NC_000004.11:g.6303618C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004780.3, RCV000238945.1,