rs1060499802

Orientation

plus

Stabilized

plus

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

Make rs1060499802(C;T)

Make rs1060499802(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

77211311

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs1060499802
dbSNP (classic)	rs1060499802
ClinGen	rs1060499802
ebi	rs1060499802
HLI	rs1060499802
Exac	rs1060499802
Gnomad	rs1060499802
Varsome	rs1060499802
LitVar	rs1060499802
Map	rs1060499802
PheGenI	rs1060499802
Biobank	rs1060499802
1000 genomes	rs1060499802
hgdp	rs1060499802
ensembl	rs1060499802
geneview	rs1060499802
scholar	rs1060499802
google	rs1060499802
pharmgkb	rs1060499802
gwascentral	rs1060499802
openSNP	rs1060499802
23andMe	rs1060499802
SNPshot	rs1060499802
SNPdbe	rs1060499802
MSV3d	rs1060499802
GWAS Ctlg	rs1060499802

Max Magnitude

0

ClinVar
Risk	rs1060499802(T;T)
Alt	rs1060499802(T;T)
Reference	Rs1060499802(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO7A
CLNDBN	Deafness, autosomal recessive 2
Reversed	0
HGVS	NC_000011.9:g.76922356C>T
CLNSRC
CLNACC	RCV000454181.1,