rs121908928

Orientation

plus

Stabilized

plus

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

Make rs121908928(A;A)

Make rs121908928(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

30878834

Gene	COCH, LOC100506071

is a	snp
is	mentioned by
dbSNP	rs121908928
dbSNP (classic)	rs121908928
ClinGen	rs121908928
ebi	rs121908928
HLI	rs121908928
Exac	rs121908928
Gnomad	rs121908928
Varsome	rs121908928
LitVar	rs121908928
Map	rs121908928
PheGenI	rs121908928
Biobank	rs121908928
1000 genomes	rs121908928
hgdp	rs121908928
ensembl	rs121908928
geneview	rs121908928
scholar	rs121908928
google	rs121908928
pharmgkb	rs121908928
gwascentral	rs121908928
openSNP	rs121908928
23andMe	rs121908928
SNPshot	rs121908928
SNPdbe	rs121908928
MSV3d	rs121908928
GWAS Ctlg	rs121908928

Max Magnitude

0

OMIM	603196
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908928(A;A) rs121908928(T;T)
Alt	rs121908928(A;A) rs121908928(T;T)
Reference	Rs121908928(G;G)
Significance	Pathogenic
Disease	Deafness not specified
Variation	info
Gene	COCH LOC100506071
CLNDBN	Deafness, autosomal dominant 9 not specified
Reversed	0
HGVS	NC_000014.8:g.31348040G>A; NC_000014.8:g.31348040G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006988.4, RCV000155766.1,