rs779077039

Orientation

plus

Stabilized

plus

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

Make rs779077039(C;T)

Make rs779077039(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

18135756

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs779077039
dbSNP (classic)	rs779077039
ClinGen	rs779077039
ebi	rs779077039
HLI	rs779077039
Exac	rs779077039
Gnomad	rs779077039
Varsome	rs779077039
LitVar	rs779077039
Map	rs779077039
PheGenI	rs779077039
Biobank	rs779077039
1000 genomes	rs779077039
hgdp	rs779077039
ensembl	rs779077039
geneview	rs779077039
scholar	rs779077039
google	rs779077039
pharmgkb	rs779077039
gwascentral	rs779077039
openSNP	rs779077039
23andMe	rs779077039
SNPshot	rs779077039
SNPdbe	rs779077039
MSV3d	rs779077039
GWAS Ctlg	rs779077039

Max Magnitude

0

ClinVar
Risk	rs779077039(T;T)
Alt	rs779077039(T;T)
Reference	Rs779077039(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18039070C>T
CLNSRC
CLNACC	RCV000417183.1,