rs184435771

Orientation

plus

Stabilized

plus

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

Make rs184435771(A;A)

Make rs184435771(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

18154714

Gene	LOC105371567, LOC105371568, MYO15A

is a	snp
is	mentioned by
dbSNP	rs184435771
dbSNP (classic)	rs184435771
ClinGen	rs184435771
ebi	rs184435771
HLI	rs184435771
Exac	rs184435771
Gnomad	rs184435771
Varsome	rs184435771
LitVar	rs184435771
Map	rs184435771
PheGenI	rs184435771
Biobank	rs184435771
1000 genomes	rs184435771
hgdp	rs184435771
ensembl	rs184435771
geneview	rs184435771
scholar	rs184435771
google	rs184435771
pharmgkb	rs184435771
gwascentral	rs184435771
openSNP	rs184435771
23andMe	rs184435771
SNPshot	rs184435771
SNPdbe	rs184435771
MSV3d	rs184435771
GWAS Ctlg	rs184435771

Max Magnitude

0

ClinVar
Risk	rs184435771(A;A)
Alt	rs184435771(A;A)
Reference	Rs184435771(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness Deafness not provided
Variation	info
Gene	MYO15A
CLNDBN	Nonsyndromic hearing loss and deafness Deafness, autosomal recessive 3 not provided
Reversed	0
HGVS	NC_000017.10:g.18058028G>A
CLNSRC
CLNACC	RCV000218811.1, RCV000225017.1, RCV000429443.1,