rs876657652

Orientation

plus

Stabilized

plus

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

Make rs876657652(C;C)

Make rs876657652(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

26193312

Gene

MYO3A

is a	snp
is	mentioned by
dbSNP	rs876657652
dbSNP (classic)	rs876657652
ClinGen	rs876657652
ebi	rs876657652
HLI	rs876657652
Exac	rs876657652
Gnomad	rs876657652
Varsome	rs876657652
LitVar	rs876657652
Map	rs876657652
PheGenI	rs876657652
Biobank	rs876657652
1000 genomes	rs876657652
hgdp	rs876657652
ensembl	rs876657652
geneview	rs876657652
scholar	rs876657652
google	rs876657652
pharmgkb	rs876657652
gwascentral	rs876657652
openSNP	rs876657652
23andMe	rs876657652
SNPshot	rs876657652
SNPdbe	rs876657652
MSV3d	rs876657652
GWAS Ctlg	rs876657652

Max Magnitude

0

ClinVar
Risk	rs876657652(C;C)
Alt	rs876657652(C;C)
Reference	Rs876657652(G;G)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MYO3A
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000010.10:g.26482241G>C
CLNSRC
CLNACC	RCV000221092.1,