rs397517287

Orientation

plus

Stabilized

plus

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

Make rs397517287(-;-)

Make rs397517287(-;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

18154142

Gene	LOC105371567, LOC105371568, MYO15A

is a	snp
is	mentioned by
dbSNP	rs397517287
dbSNP (classic)	rs397517287
ClinGen	rs397517287
ebi	rs397517287
HLI	rs397517287
Exac	rs397517287
Gnomad	rs397517287
Varsome	rs397517287
LitVar	rs397517287
Map	rs397517287
PheGenI	rs397517287
Biobank	rs397517287
1000 genomes	rs397517287
hgdp	rs397517287
ensembl	rs397517287
geneview	rs397517287
scholar	rs397517287
google	rs397517287
pharmgkb	rs397517287
gwascentral	rs397517287
openSNP	rs397517287
23andMe	rs397517287
SNPshot	rs397517287
SNPdbe	rs397517287
MSV3d	rs397517287
GWAS Ctlg	rs397517287

Max Magnitude

0

ClinVar
Risk	rs397517287(-;-)
Alt	rs397517287(-;-)
Reference	Rs397517287(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.18057456delC
CLNSRC	ClinVar
CLNACC	RCV000038989.2,