rs397517286

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(D;D)	0	common genotype

Make rs397517286(-;C)

Make rs397517286(C;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

18149265

Gene	LOC105371568, MYO15A

is a	snp
is	mentioned by
dbSNP	rs397517286
dbSNP (classic)	rs397517286
ClinGen	rs397517286
ebi	rs397517286
HLI	rs397517286
Exac	rs397517286
Gnomad	rs397517286
Varsome	rs397517286
LitVar	rs397517286
Map	rs397517286
PheGenI	rs397517286
Biobank	rs397517286
1000 genomes	rs397517286
hgdp	rs397517286
ensembl	rs397517286
geneview	rs397517286
scholar	rs397517286
google	rs397517286
pharmgkb	rs397517286
gwascentral	rs397517286
openSNP	rs397517286
23andMe	rs397517286
SNPshot	rs397517286
SNPdbe	rs397517286
MSV3d	rs397517286
GWAS Ctlg	rs397517286

Max Magnitude

0

ClinVar
Risk	rs397517286(C;C)
Alt	rs397517286(C;C)
Reference	Rs397517286(-;-)
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.18052579dupC
CLNSRC	ClinVar
CLNACC	RCV000038981.2,