rs1060499651

Orientation

plus

Stabilized

plus

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

Make rs1060499651(-;-)

Make rs1060499651(-;GT)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

77156754

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs1060499651
dbSNP (classic)	rs1060499651
ClinGen	rs1060499651
ebi	rs1060499651
HLI	rs1060499651
Exac	rs1060499651
Gnomad	rs1060499651
Varsome	rs1060499651
LitVar	rs1060499651
Map	rs1060499651
PheGenI	rs1060499651
Biobank	rs1060499651
1000 genomes	rs1060499651
hgdp	rs1060499651
ensembl	rs1060499651
geneview	rs1060499651
scholar	rs1060499651
google	rs1060499651
pharmgkb	rs1060499651
gwascentral	rs1060499651
openSNP	rs1060499651
23andMe	rs1060499651
SNPshot	rs1060499651
SNPdbe	rs1060499651
MSV3d	rs1060499651
GWAS Ctlg	rs1060499651

Max Magnitude

0

ClinVar
Risk	rs1060499651(-;-)
Alt	rs1060499651(-;-)
Reference	Rs1060499651(GT;GT)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO7A
CLNDBN	Deafness, autosomal recessive 2
Reversed	0
HGVS	NC_000011.9:g.76867800_76867801delGT
CLNSRC
CLNACC	RCV000449499.1,