rs111033239

Orientation

plus

Stabilized

plus

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

Make rs111033239(-;-)

Make rs111033239(-;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77189372

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033239
dbSNP (classic)	rs111033239
ClinGen	rs111033239
ebi	rs111033239
HLI	rs111033239
Exac	rs111033239
Gnomad	rs111033239
Varsome	rs111033239
LitVar	rs111033239
Map	rs111033239
PheGenI	rs111033239
Biobank	rs111033239
1000 genomes	rs111033239
hgdp	rs111033239
ensembl	rs111033239
geneview	rs111033239
scholar	rs111033239
google	rs111033239
pharmgkb	rs111033239
gwascentral	rs111033239
openSNP	rs111033239
23andMe	rs111033239
SNPshot	rs111033239
SNPdbe	rs111033239
MSV3d	rs111033239
GWAS Ctlg	rs111033239

Max Magnitude

0

ClinVar
Risk	rs111033239(-;-)
Alt	rs111033239(-;-)
Reference	Rs111033239(C;C)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76900417delC
CLNSRC	ClinVar
CLNACC	RCV000036113.2,