rs111033389

Orientation

plus

Stabilized

plus

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

Make rs111033389(A;A)

Make rs111033389(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77162989

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033389
dbSNP (classic)	rs111033389
ClinGen	rs111033389
ebi	rs111033389
HLI	rs111033389
Exac	rs111033389
Gnomad	rs111033389
Varsome	rs111033389
LitVar	rs111033389
Map	rs111033389
PheGenI	rs111033389
Biobank	rs111033389
1000 genomes	rs111033389
hgdp	rs111033389
ensembl	rs111033389
geneview	rs111033389
scholar	rs111033389
google	rs111033389
pharmgkb	rs111033389
gwascentral	rs111033389
openSNP	rs111033389
23andMe	rs111033389
SNPshot	rs111033389
SNPdbe	rs111033389
MSV3d	rs111033389
GWAS Ctlg	rs111033389

Max Magnitude

0

ClinVar
Risk	rs111033389(A;A)
Alt	rs111033389(A;A)
Reference	Rs111033389(G;G)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76874035G>A
CLNSRC	ClinVar
CLNACC	RCV000036059.2,