rs111033215

Orientation

plus

Stabilized

plus

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

Make rs111033215(A;A)

Make rs111033215(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

77206108

Gene

MYO7A

is a	snp
is	mentioned by
dbSNP	rs111033215
dbSNP (classic)	rs111033215
ClinGen	rs111033215
ebi	rs111033215
HLI	rs111033215
Exac	rs111033215
Gnomad	rs111033215
Varsome	rs111033215
LitVar	rs111033215
Map	rs111033215
PheGenI	rs111033215
Biobank	rs111033215
1000 genomes	rs111033215
hgdp	rs111033215
ensembl	rs111033215
geneview	rs111033215
scholar	rs111033215
google	rs111033215
pharmgkb	rs111033215
gwascentral	rs111033215
openSNP	rs111033215
23andMe	rs111033215
SNPshot	rs111033215
SNPdbe	rs111033215
MSV3d	rs111033215
GWAS Ctlg	rs111033215

Max Magnitude

0

ClinVar
Risk	rs111033215(A;A)
Alt	rs111033215(A;A)
Reference	Rs111033215(G;G)
Significance	Pathogenic
Disease	Usher syndrome not provided
Variation	info
Gene	MYO7A
CLNDBN	Usher syndrome, type 1 not provided
Reversed	0
HGVS	NC_000011.9:g.76917153G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000036199.3, RCV000413954.1,