rs727503315

Orientation

plus

Stabilized

plus

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

Make rs727503315(-;-)

Make rs727503315(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

18150442

Gene	LOC105371568, MYO15A

is a	snp
is	mentioned by
dbSNP	rs727503315
dbSNP (classic)	rs727503315
ClinGen	rs727503315
ebi	rs727503315
HLI	rs727503315
Exac	rs727503315
Gnomad	rs727503315
Varsome	rs727503315
LitVar	rs727503315
Map	rs727503315
PheGenI	rs727503315
Biobank	rs727503315
1000 genomes	rs727503315
hgdp	rs727503315
ensembl	rs727503315
geneview	rs727503315
scholar	rs727503315
google	rs727503315
pharmgkb	rs727503315
gwascentral	rs727503315
openSNP	rs727503315
23andMe	rs727503315
SNPshot	rs727503315
SNPdbe	rs727503315
MSV3d	rs727503315
GWAS Ctlg	rs727503315

Max Magnitude

0

ClinVar
Risk	rs727503315(-;-)
Alt	rs727503315(-;-)
Reference	Rs727503315(C;C)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness not provided
Variation	info
Gene	MYO15A
CLNDBN	Nonsyndromic hearing loss and deafness not provided
Reversed	0
HGVS	NC_000017.10:g.18053756delC
CLNSRC
CLNACC	RCV000151407.1, RCV000255552.2,