rs121908931

Orientation

plus

Stabilized

plus

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

Make rs121908931(A;A)

Make rs121908931(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

30878926

Gene	COCH, LOC100506071

is a	snp
is	mentioned by
dbSNP	rs121908931
dbSNP (classic)	rs121908931
ClinGen	rs121908931
ebi	rs121908931
HLI	rs121908931
Exac	rs121908931
Gnomad	rs121908931
Varsome	rs121908931
LitVar	rs121908931
Map	rs121908931
PheGenI	rs121908931
Biobank	rs121908931
1000 genomes	rs121908931
hgdp	rs121908931
ensembl	rs121908931
geneview	rs121908931
scholar	rs121908931
google	rs121908931
pharmgkb	rs121908931
gwascentral	rs121908931
openSNP	rs121908931
23andMe	rs121908931
SNPshot	rs121908931
SNPdbe	rs121908931
MSV3d	rs121908931
GWAS Ctlg	rs121908931

Max Magnitude

0

OMIM	603196
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121908931(A;A)
Alt	rs121908931(A;A)
Reference	Rs121908931(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	COCH LOC100506071
CLNDBN	Deafness, autosomal dominant 9
Reversed	0
HGVS	NC_000014.8:g.31348132G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006992.3,