rs111033175

Orientation

plus

Stabilized

plus

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

Make rs111033175(A;G)

Make rs111033175(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77208781

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033175
dbSNP (classic)	rs111033175
ClinGen	rs111033175
ebi	rs111033175
HLI	rs111033175
Exac	rs111033175
Gnomad	rs111033175
Varsome	rs111033175
LitVar	rs111033175
Map	rs111033175
PheGenI	rs111033175
Biobank	rs111033175
1000 genomes	rs111033175
hgdp	rs111033175
ensembl	rs111033175
geneview	rs111033175
scholar	rs111033175
google	rs111033175
pharmgkb	rs111033175
gwascentral	rs111033175
openSNP	rs111033175
23andMe	rs111033175
SNPshot	rs111033175
SNPdbe	rs111033175
MSV3d	rs111033175
GWAS Ctlg	rs111033175

Max Magnitude

0

ClinVar
Risk	rs111033175(G;G)
Alt	rs111033175(G;G)
Reference	Rs111033175(A;A)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76919826A>G
CLNSRC	ClinVar
CLNACC	RCV000036219.2,