rs111033486

Orientation

plus

Stabilized

plus

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

Make rs111033486(A;G)

Make rs111033486(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77156900

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033486
dbSNP (classic)	rs111033486
ClinGen	rs111033486
ebi	rs111033486
HLI	rs111033486
Exac	rs111033486
Gnomad	rs111033486
Varsome	rs111033486
LitVar	rs111033486
Map	rs111033486
PheGenI	rs111033486
Biobank	rs111033486
1000 genomes	rs111033486
hgdp	rs111033486
ensembl	rs111033486
geneview	rs111033486
scholar	rs111033486
google	rs111033486
pharmgkb	rs111033486
gwascentral	rs111033486
openSNP	rs111033486
23andMe	rs111033486
SNPshot	rs111033486
SNPdbe	rs111033486
MSV3d	rs111033486
GWAS Ctlg	rs111033486

Max Magnitude

0

ClinVar
Risk	rs111033486(G;G)
Alt	rs111033486(G;G)
Reference	Rs111033486(A;A)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76867946A>G
CLNSRC	ClinVar
CLNACC	RCV000036230.2,