rs878853226

Orientation

plus

Stabilized

plus

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

Make rs878853226(C;T)

Make rs878853226(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

14

Position

30885994

Gene	COCH, LOC100506071

is a	snp
is	mentioned by
dbSNP	rs878853226
dbSNP (classic)	rs878853226
ClinGen	rs878853226
ebi	rs878853226
HLI	rs878853226
Exac	rs878853226
Gnomad	rs878853226
Varsome	rs878853226
LitVar	rs878853226
Map	rs878853226
PheGenI	rs878853226
Biobank	rs878853226
1000 genomes	rs878853226
hgdp	rs878853226
ensembl	rs878853226
geneview	rs878853226
scholar	rs878853226
google	rs878853226
pharmgkb	rs878853226
gwascentral	rs878853226
openSNP	rs878853226
23andMe	rs878853226
SNPshot	rs878853226
SNPdbe	rs878853226
MSV3d	rs878853226
GWAS Ctlg	rs878853226

Max Magnitude

0

ClinVar
Risk	rs878853226(T;T)
Alt	rs878853226(T;T)
Reference	Rs878853226(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	COCH LOC100506071
CLNDBN	Deafness, autosomal dominant 9
Reversed	0
HGVS	NC_000014.8:g.31355200C>T
CLNSRC
CLNACC	RCV000225026.1,