rs121912618

Orientation

plus

Stabilized

plus

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

Make rs121912618(A;A)

Make rs121912618(A;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

6302371

Gene	LOC107986257, WFS1

is a	snp
is	mentioned by
dbSNP	rs121912618
dbSNP (classic)	rs121912618
ClinGen	rs121912618
ebi	rs121912618
HLI	rs121912618
Exac	rs121912618
Gnomad	rs121912618
Varsome	rs121912618
LitVar	rs121912618
Map	rs121912618
PheGenI	rs121912618
Biobank	rs121912618
1000 genomes	rs121912618
hgdp	rs121912618
ensembl	rs121912618
geneview	rs121912618
scholar	rs121912618
google	rs121912618
pharmgkb	rs121912618
gwascentral	rs121912618
openSNP	rs121912618
23andMe	rs121912618
SNPshot	rs121912618
SNPdbe	rs121912618
MSV3d	rs121912618
GWAS Ctlg	rs121912618

Max Magnitude

0

OMIM	606201
Desc
Variant	0023
Related	also

ClinVar
Risk	rs121912618(A;A)
Alt	rs121912618(A;A)
Reference	Rs121912618(G;G)
Significance	Pathogenic
Disease	WFS1-Related Disorders WFS1-Related Spectrum Disorders Nonsyndromic Hearing Loss not specified
Variation	info
Gene	WFS1
CLNDBN	WFS1-Related Disorders WFS1-Related Spectrum Disorders Nonsyndromic Hearing Loss, Dominant not specified
Reversed	0
HGVS	NC_000004.11:g.6304098G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000004787.3, RCV000275899.1, RCV000367914.1, RCV000480362.1,