rs111033192

Orientation

plus

Stabilized

plus

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

Make rs111033192(A;A)

Make rs111033192(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77207370

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033192
dbSNP (classic)	rs111033192
ClinGen	rs111033192
ebi	rs111033192
HLI	rs111033192
Exac	rs111033192
Gnomad	rs111033192
Varsome	rs111033192
LitVar	rs111033192
Map	rs111033192
PheGenI	rs111033192
Biobank	rs111033192
1000 genomes	rs111033192
hgdp	rs111033192
ensembl	rs111033192
geneview	rs111033192
scholar	rs111033192
google	rs111033192
pharmgkb	rs111033192
gwascentral	rs111033192
openSNP	rs111033192
23andMe	rs111033192
SNPshot	rs111033192
SNPdbe	rs111033192
MSV3d	rs111033192
GWAS Ctlg	rs111033192

Max Magnitude

0

ClinVar
Risk	rs111033192(A;A) rs111033192(T;T)
Alt	rs111033192(A;A) rs111033192(T;T)
Reference	Rs111033192(G;G)
Significance	Pathogenic
Disease	not specified Usher syndrome MYO7A-Related Disorders
Variation	info
Gene	MYO7A
CLNDBN	not specified Usher syndrome, type 1 MYO7A-Related Disorders
Reversed	0
HGVS	NC_000011.9:g.76918415G>A; NC_000011.9:g.76918415G>T
CLNSRC	ClinVar
CLNACC	RCV000036204.2, RCV000036205.2, RCV000388623.1,