rs111033182

Orientation

plus

Stabilized

plus

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

Make rs111033182(C;T)

Make rs111033182(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77202357

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033182
dbSNP (classic)	rs111033182
ClinGen	rs111033182
ebi	rs111033182
HLI	rs111033182
Exac	rs111033182
Gnomad	rs111033182
Varsome	rs111033182
LitVar	rs111033182
Map	rs111033182
PheGenI	rs111033182
Biobank	rs111033182
1000 genomes	rs111033182
hgdp	rs111033182
ensembl	rs111033182
geneview	rs111033182
scholar	rs111033182
google	rs111033182
pharmgkb	rs111033182
gwascentral	rs111033182
openSNP	rs111033182
23andMe	rs111033182
SNPshot	rs111033182
SNPdbe	rs111033182
MSV3d	rs111033182
GWAS Ctlg	rs111033182

Max Magnitude

0

ClinVar
Risk	rs111033182(T;T)
Alt	rs111033182(T;T)
Reference	Rs111033182(C;C)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76913402C>T
CLNSRC	ClinVar
CLNACC	RCV000036175.2,