rs1060499798

Orientation

plus

Stabilized

plus

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

Make rs1060499798(A;A)

Make rs1060499798(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

18132486

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs1060499798
dbSNP (classic)	rs1060499798
ClinGen	rs1060499798
ebi	rs1060499798
HLI	rs1060499798
Exac	rs1060499798
Gnomad	rs1060499798
Varsome	rs1060499798
LitVar	rs1060499798
Map	rs1060499798
PheGenI	rs1060499798
Biobank	rs1060499798
1000 genomes	rs1060499798
hgdp	rs1060499798
ensembl	rs1060499798
geneview	rs1060499798
scholar	rs1060499798
google	rs1060499798
pharmgkb	rs1060499798
gwascentral	rs1060499798
openSNP	rs1060499798
23andMe	rs1060499798
SNPshot	rs1060499798
SNPdbe	rs1060499798
MSV3d	rs1060499798
GWAS Ctlg	rs1060499798

Max Magnitude

0

ClinVar
Risk	rs1060499798(A;A)
Alt	rs1060499798(A;A)
Reference	Rs1060499798(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18035800G>A
CLNSRC
CLNACC	RCV000454215.1,