rs1060499803

Orientation

plus

Stabilized

plus

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

Make rs1060499803(A;G)

Make rs1060499803(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

77194352

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs1060499803
dbSNP (classic)	rs1060499803
ClinGen	rs1060499803
ebi	rs1060499803
HLI	rs1060499803
Exac	rs1060499803
Gnomad	rs1060499803
Varsome	rs1060499803
LitVar	rs1060499803
Map	rs1060499803
PheGenI	rs1060499803
Biobank	rs1060499803
1000 genomes	rs1060499803
hgdp	rs1060499803
ensembl	rs1060499803
geneview	rs1060499803
scholar	rs1060499803
google	rs1060499803
pharmgkb	rs1060499803
gwascentral	rs1060499803
openSNP	rs1060499803
23andMe	rs1060499803
SNPshot	rs1060499803
SNPdbe	rs1060499803
MSV3d	rs1060499803
GWAS Ctlg	rs1060499803

Max Magnitude

0

ClinVar
Risk	rs1060499803(G;G)
Alt	rs1060499803(G;G)
Reference	Rs1060499803(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO7A
CLNDBN	Deafness, autosomal recessive 2
Reversed	0
HGVS	NC_000011.9:g.76905397A>G
CLNSRC
CLNACC	RCV000454153.1,