rs727503316

Orientation

plus

Stabilized

plus

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

Make rs727503316(A;A)

Make rs727503316(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

18151952

Gene	LOC105371568, MYO15A

is a	snp
is	mentioned by
dbSNP	rs727503316
dbSNP (classic)	rs727503316
ClinGen	rs727503316
ebi	rs727503316
HLI	rs727503316
Exac	rs727503316
Gnomad	rs727503316
Varsome	rs727503316
LitVar	rs727503316
Map	rs727503316
PheGenI	rs727503316
Biobank	rs727503316
1000 genomes	rs727503316
hgdp	rs727503316
ensembl	rs727503316
geneview	rs727503316
scholar	rs727503316
google	rs727503316
pharmgkb	rs727503316
gwascentral	rs727503316
openSNP	rs727503316
23andMe	rs727503316
SNPshot	rs727503316
SNPdbe	rs727503316
MSV3d	rs727503316
GWAS Ctlg	rs727503316

Max Magnitude

0

ClinVar
Risk	rs727503316(A;A)
Alt	rs727503316(A;A)
Reference	Rs727503316(G;G)
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.18055266G>A
CLNSRC
CLNACC	RCV000151411.1,