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rs797044510

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044510(A;A)
Make rs797044510(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position77156092
GeneMYO7A
is asnp
is mentioned by
dbSNPrs797044510
ebirs797044510
HLIrs797044510
Exacrs797044510
Varsomers797044510
Maprs797044510
PheGenIrs797044510
hapmaprs797044510
1000 genomesrs797044510
hgdprs797044510
ensemblrs797044510
gopubmedrs797044510
geneviewrs797044510
scholarrs797044510
googlers797044510
pharmgkbrs797044510
gwascentralrs797044510
openSNPrs797044510
23andMers797044510
23andMe allrs797044510
SNP Nexus

SNPshotrs797044510
SNPdbers797044510
MSV3drs797044510
GWAS Ctlgrs797044510
Max Magnitude0
ClinVar
Risk rs797044510(A;A)
Alt rs797044510(A;A)
Reference rs797044510(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76867138G>A
CLNSRC
CLNACC RCV000154316.1,