rs397517285

Orientation

plus

Stabilized

plus

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

Make rs397517285(A;A)

Make rs397517285(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

18148784

Gene	LOC105371568, MYO15A

is a	snp
is	mentioned by
dbSNP	rs397517285
dbSNP (classic)	rs397517285
ClinGen	rs397517285
ebi	rs397517285
HLI	rs397517285
Exac	rs397517285
Gnomad	rs397517285
Varsome	rs397517285
LitVar	rs397517285
Map	rs397517285
PheGenI	rs397517285
Biobank	rs397517285
1000 genomes	rs397517285
hgdp	rs397517285
ensembl	rs397517285
geneview	rs397517285
scholar	rs397517285
google	rs397517285
pharmgkb	rs397517285
gwascentral	rs397517285
openSNP	rs397517285
23andMe	rs397517285
SNPshot	rs397517285
SNPdbe	rs397517285
MSV3d	rs397517285
GWAS Ctlg	rs397517285

Max Magnitude

0

ClinVar
Risk	rs397517285(A;A)
Alt	rs397517285(A;A)
Reference	Rs397517285(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.18052098G>A
CLNSRC
CLNACC	RCV000038980.2,