rs876657710

Orientation

plus

Stabilized

plus

Make rs876657710(C;G)

Make rs876657710(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

6

Position

75832908

Gene

MYO6

is a	snp
is	mentioned by
dbSNP	rs876657710
dbSNP (classic)	rs876657710
ClinGen	rs876657710
ebi	rs876657710
HLI	rs876657710
Exac	rs876657710
Gnomad	rs876657710
Varsome	rs876657710
LitVar	rs876657710
Map	rs876657710
PheGenI	rs876657710
Biobank	rs876657710
1000 genomes	rs876657710
hgdp	rs876657710
ensembl	rs876657710
geneview	rs876657710
scholar	rs876657710
google	rs876657710
pharmgkb	rs876657710
gwascentral	rs876657710
openSNP	rs876657710
23andMe	rs876657710
SNPshot	rs876657710
SNPdbe	rs876657710
MSV3d	rs876657710
GWAS Ctlg	rs876657710

Max Magnitude

0

ClinVar
Risk	rs876657710(G;G)
Alt	rs876657710(G;G)
Reference	Rs876657710(C;C)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MYO6
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000006.11:g.76542625C>G
CLNSRC
CLNACC	RCV000216690.1,