rs111033337

Orientation

plus

Stabilized

plus

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

Make rs111033337(A;C)

Make rs111033337(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

77198493

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033337
dbSNP (classic)	rs111033337
ClinGen	rs111033337
ebi	rs111033337
HLI	rs111033337
Exac	rs111033337
Gnomad	rs111033337
Varsome	rs111033337
LitVar	rs111033337
Map	rs111033337
PheGenI	rs111033337
Biobank	rs111033337
1000 genomes	rs111033337
hgdp	rs111033337
ensembl	rs111033337
geneview	rs111033337
scholar	rs111033337
google	rs111033337
pharmgkb	rs111033337
gwascentral	rs111033337
openSNP	rs111033337
23andMe	rs111033337
SNPshot	rs111033337
SNPdbe	rs111033337
MSV3d	rs111033337
GWAS Ctlg	rs111033337

Max Magnitude

0

ClinVar
Risk	rs111033337(C;C)
Alt	rs111033337(C;C)
Reference	Rs111033337(A;A)
Significance	Probable-Pathogenic
Disease	Usher syndrome
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1
Reversed	0
HGVS	NC_000011.9:g.76909538A>C
CLNSRC	ClinVar
CLNACC	RCV000036144.2,