rs794729637

Orientation

plus

Stabilized

plus

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

Make rs794729637(-;G)

Make rs794729637(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

18122111

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs794729637
dbSNP (classic)	rs794729637
ClinGen	rs794729637
ebi	rs794729637
HLI	rs794729637
Exac	rs794729637
Gnomad	rs794729637
Varsome	rs794729637
LitVar	rs794729637
Map	rs794729637
PheGenI	rs794729637
Biobank	rs794729637
1000 genomes	rs794729637
hgdp	rs794729637
ensembl	rs794729637
geneview	rs794729637
scholar	rs794729637
google	rs794729637
pharmgkb	rs794729637
gwascentral	rs794729637
openSNP	rs794729637
23andMe	rs794729637
SNPshot	rs794729637
SNPdbe	rs794729637
MSV3d	rs794729637
GWAS Ctlg	rs794729637

Max Magnitude

0

ClinVar
Risk	rs794729637(G;G)
Alt	rs794729637(G;G)
Reference	Rs794729637(-;-)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18025425dupG
CLNSRC
CLNACC	RCV000185530.2,