rs876657653

Orientation

plus

Stabilized

plus

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

Make rs876657653(C;T)

Make rs876657653(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

6

Position

75890237

Gene

MYO6

is a	snp
is	mentioned by
dbSNP	rs876657653
dbSNP (classic)	rs876657653
ClinGen	rs876657653
ebi	rs876657653
HLI	rs876657653
Exac	rs876657653
Gnomad	rs876657653
Varsome	rs876657653
LitVar	rs876657653
Map	rs876657653
PheGenI	rs876657653
Biobank	rs876657653
1000 genomes	rs876657653
hgdp	rs876657653
ensembl	rs876657653
geneview	rs876657653
scholar	rs876657653
google	rs876657653
pharmgkb	rs876657653
gwascentral	rs876657653
openSNP	rs876657653
23andMe	rs876657653
SNPshot	rs876657653
SNPdbe	rs876657653
MSV3d	rs876657653
GWAS Ctlg	rs876657653

Max Magnitude

0

ClinVar
Risk	rs876657653(T;T)
Alt	rs876657653(T;T)
Reference	Rs876657653(C;C)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MYO6
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000006.11:g.76599954C>T
CLNSRC
CLNACC	RCV000215443.1,