rs373462792

Orientation

plus

Stabilized

plus

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

Make rs373462792(C;T)

Make rs373462792(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

18157209

Gene	LOC105371567, MYO15A

is a	snp
is	mentioned by
dbSNP	rs373462792
dbSNP (classic)	rs373462792
ClinGen	rs373462792
ebi	rs373462792
HLI	rs373462792
Exac	rs373462792
Gnomad	rs373462792
Varsome	rs373462792
LitVar	rs373462792
Map	rs373462792
PheGenI	rs373462792
Biobank	rs373462792
1000 genomes	rs373462792
hgdp	rs373462792
ensembl	rs373462792
geneview	rs373462792
scholar	rs373462792
google	rs373462792
pharmgkb	rs373462792
gwascentral	rs373462792
openSNP	rs373462792
23andMe	rs373462792
SNPshot	rs373462792
SNPdbe	rs373462792
MSV3d	rs373462792
GWAS Ctlg	rs373462792

Max Magnitude

0

ClinVar
Risk	rs373462792(T;T)
Alt	rs373462792(T;T)
Reference	Rs373462792(C;C)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MYO15A
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000017.10:g.18060523C>T
CLNSRC	ClinVar
CLNACC	RCV000038995.3,