rs111033404

Orientation

plus

Stabilized

plus

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

Make rs111033404(C;C)

Make rs111033404(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77174915

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033404
dbSNP (classic)	rs111033404
ClinGen	rs111033404
ebi	rs111033404
HLI	rs111033404
Exac	rs111033404
Gnomad	rs111033404
Varsome	rs111033404
LitVar	rs111033404
Map	rs111033404
PheGenI	rs111033404
Biobank	rs111033404
1000 genomes	rs111033404
hgdp	rs111033404
ensembl	rs111033404
geneview	rs111033404
scholar	rs111033404
google	rs111033404
pharmgkb	rs111033404
gwascentral	rs111033404
openSNP	rs111033404
23andMe	rs111033404
SNPshot	rs111033404
SNPdbe	rs111033404
MSV3d	rs111033404
GWAS Ctlg	rs111033404

Max Magnitude

0

ClinVar
Risk	rs111033404(A;A) rs111033404(C;C)
Alt	rs111033404(A;A) rs111033404(C;C)
Reference	Rs111033404(G;G)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76885961G>A; NC_000011.9:g.76885961G>C
CLNSRC	ClinVar
CLNACC	RCV000036075.2, RCV000036076.2,