rs111033276

Orientation

plus

Stabilized

plus

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

Make rs111033276(-;C)

Make rs111033276(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77203099

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033276
dbSNP (classic)	rs111033276
ClinGen	rs111033276
ebi	rs111033276
HLI	rs111033276
Exac	rs111033276
Gnomad	rs111033276
Varsome	rs111033276
LitVar	rs111033276
Map	rs111033276
PheGenI	rs111033276
Biobank	rs111033276
1000 genomes	rs111033276
hgdp	rs111033276
ensembl	rs111033276
geneview	rs111033276
scholar	rs111033276
google	rs111033276
pharmgkb	rs111033276
gwascentral	rs111033276
openSNP	rs111033276
23andMe	rs111033276
SNPshot	rs111033276
SNPdbe	rs111033276
MSV3d	rs111033276
GWAS Ctlg	rs111033276

Max Magnitude

0

ClinVar
Risk	rs111033276(C;C)
Alt	rs111033276(C;C)
Reference	Rs111033276(-;-)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76914144dupC
CLNSRC	ClinVar
CLNACC	RCV000036180.2,