rs779760634

Orientation

plus

Stabilized

plus

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

Make rs779760634(C;T)

Make rs779760634(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

114423524

Gene

WHRN

is a	snp
is	mentioned by
dbSNP	rs779760634
dbSNP (classic)	rs779760634
ClinGen	rs779760634
ebi	rs779760634
HLI	rs779760634
Exac	rs779760634
Gnomad	rs779760634
Varsome	rs779760634
LitVar	rs779760634
Map	rs779760634
PheGenI	rs779760634
Biobank	rs779760634
1000 genomes	rs779760634
hgdp	rs779760634
ensembl	rs779760634
geneview	rs779760634
scholar	rs779760634
google	rs779760634
pharmgkb	rs779760634
gwascentral	rs779760634
openSNP	rs779760634
23andMe	rs779760634
SNPshot	rs779760634
SNPdbe	rs779760634
MSV3d	rs779760634
GWAS Ctlg	rs779760634

Max Magnitude

0

ClinVar
Risk	rs779760634(T;T)
Alt	rs779760634(T;T)
Reference	Rs779760634(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	WHRN DFNB31
CLNDBN	Deafness, autosomal recessive 31
Reversed	0
HGVS	NC_000009.11:g.117185804C>T
CLNSRC
CLNACC	RCV000179947.1,