rs111033403

Orientation

plus

Stabilized

plus

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

Make rs111033403(A;A)

Make rs111033403(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77156018

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033403
dbSNP (classic)	rs111033403
ClinGen	rs111033403
ebi	rs111033403
HLI	rs111033403
Exac	rs111033403
Gnomad	rs111033403
Varsome	rs111033403
LitVar	rs111033403
Map	rs111033403
PheGenI	rs111033403
Biobank	rs111033403
1000 genomes	rs111033403
hgdp	rs111033403
ensembl	rs111033403
geneview	rs111033403
scholar	rs111033403
google	rs111033403
pharmgkb	rs111033403
gwascentral	rs111033403
openSNP	rs111033403
23andMe	rs111033403
SNPshot	rs111033403
SNPdbe	rs111033403
MSV3d	rs111033403
GWAS Ctlg	rs111033403

Max Magnitude

0

ClinVar
Risk	rs111033403(A;A) rs111033403(T;T)
Alt	rs111033403(A;A) rs111033403(T;T)
Reference	Rs111033403(C;C)
Significance	Probable-Pathogenic
Disease	not specified Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	not specified Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76867064C>A; NC_000011.9:g.76867064C>T
CLNSRC	ClinVar
CLNACC	RCV000151476.1, RCV000036132.2,