rs1060499800

Orientation

plus

Stabilized

plus

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

Make rs1060499800(-;-)

Make rs1060499800(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

77179069

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs1060499800
dbSNP (classic)	rs1060499800
ClinGen	rs1060499800
ebi	rs1060499800
HLI	rs1060499800
Exac	rs1060499800
Gnomad	rs1060499800
Varsome	rs1060499800
LitVar	rs1060499800
Map	rs1060499800
PheGenI	rs1060499800
Biobank	rs1060499800
1000 genomes	rs1060499800
hgdp	rs1060499800
ensembl	rs1060499800
geneview	rs1060499800
scholar	rs1060499800
google	rs1060499800
pharmgkb	rs1060499800
gwascentral	rs1060499800
openSNP	rs1060499800
23andMe	rs1060499800
SNPshot	rs1060499800
SNPdbe	rs1060499800
MSV3d	rs1060499800
GWAS Ctlg	rs1060499800

Max Magnitude

0

ClinVar
Risk	rs1060499800(-;-)
Alt	rs1060499800(-;-)
Reference	Rs1060499800(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO7A
CLNDBN	Deafness, autosomal recessive 2
Reversed	0
HGVS	NC_000011.9:g.76890115delC
CLNSRC
CLNACC	RCV000454349.1,