rs111033238

Orientation

plus

Stabilized

plus

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

Make rs111033238(-;-)

Make rs111033238(-;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77156771

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033238
dbSNP (classic)	rs111033238
ClinGen	rs111033238
ebi	rs111033238
HLI	rs111033238
Exac	rs111033238
Gnomad	rs111033238
Varsome	rs111033238
LitVar	rs111033238
Map	rs111033238
PheGenI	rs111033238
Biobank	rs111033238
1000 genomes	rs111033238
hgdp	rs111033238
ensembl	rs111033238
geneview	rs111033238
scholar	rs111033238
google	rs111033238
pharmgkb	rs111033238
gwascentral	rs111033238
openSNP	rs111033238
23andMe	rs111033238
SNPshot	rs111033238
SNPdbe	rs111033238
MSV3d	rs111033238
GWAS Ctlg	rs111033238

Max Magnitude

0

ClinVar
Risk	rs111033238(-;-)
Alt	rs111033238(-;-)
Reference	Rs111033238(C;C)
Significance	Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76867817delC
CLNSRC	ClinVar
CLNACC	RCV000036206.2,