rs760980785

Orientation

plus

Stabilized

plus

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

Make rs760980785(A;A)

Make rs760980785(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

18146035

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs760980785
dbSNP (classic)	rs760980785
ClinGen	rs760980785
ebi	rs760980785
HLI	rs760980785
Exac	rs760980785
Gnomad	rs760980785
Varsome	rs760980785
LitVar	rs760980785
Map	rs760980785
PheGenI	rs760980785
Biobank	rs760980785
1000 genomes	rs760980785
hgdp	rs760980785
ensembl	rs760980785
geneview	rs760980785
scholar	rs760980785
google	rs760980785
pharmgkb	rs760980785
gwascentral	rs760980785
openSNP	rs760980785
23andMe	rs760980785
SNPshot	rs760980785
SNPdbe	rs760980785
MSV3d	rs760980785
GWAS Ctlg	rs760980785

Max Magnitude

0

ClinVar
Risk	rs760980785(A;A)
Alt	rs760980785(A;A)
Reference	Rs760980785(G;G)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	MYO15A
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000017.10:g.18049349G>A
CLNSRC
CLNACC	RCV000215334.1,