rs121908929

Orientation

plus

Stabilized

plus

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

Make rs121908929(C;C)

Make rs121908929(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

30878920

Gene	COCH, LOC100506071

is a	snp
is	mentioned by
dbSNP	rs121908929
dbSNP (classic)	rs121908929
ClinGen	rs121908929
ebi	rs121908929
HLI	rs121908929
Exac	rs121908929
Gnomad	rs121908929
Varsome	rs121908929
LitVar	rs121908929
Map	rs121908929
PheGenI	rs121908929
Biobank	rs121908929
1000 genomes	rs121908929
hgdp	rs121908929
ensembl	rs121908929
geneview	rs121908929
scholar	rs121908929
google	rs121908929
pharmgkb	rs121908929
gwascentral	rs121908929
openSNP	rs121908929
23andMe	rs121908929
SNPshot	rs121908929
SNPdbe	rs121908929
MSV3d	rs121908929
GWAS Ctlg	rs121908929

Max Magnitude

0

OMIM	603196
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121908929(C;C)
Alt	rs121908929(C;C)
Reference	Rs121908929(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	COCH LOC100506071
CLNDBN	Deafness, autosomal dominant 9
Reversed	0
HGVS	NC_000014.8:g.31348126T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006989.4,