rs111033284

Orientation

plus

Stabilized

plus

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

Make rs111033284(A;A)

Make rs111033284(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77156991

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033284
dbSNP (classic)	rs111033284
ClinGen	rs111033284
ebi	rs111033284
HLI	rs111033284
Exac	rs111033284
Gnomad	rs111033284
Varsome	rs111033284
LitVar	rs111033284
Map	rs111033284
PheGenI	rs111033284
Biobank	rs111033284
1000 genomes	rs111033284
hgdp	rs111033284
ensembl	rs111033284
geneview	rs111033284
scholar	rs111033284
google	rs111033284
pharmgkb	rs111033284
gwascentral	rs111033284
openSNP	rs111033284
23andMe	rs111033284
SNPshot	rs111033284
SNPdbe	rs111033284
MSV3d	rs111033284
GWAS Ctlg	rs111033284

Max Magnitude

0

ClinVar
Risk	rs111033284(A;A)
Alt	rs111033284(A;A)
Reference	Rs111033284(G;G)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76868037G>A
CLNSRC	ClinVar
CLNACC	RCV000036247.2,