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rs527236085

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236085(G;T)
Make rs527236085(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position77162965
GeneMYO7A
is asnp
is mentioned by
dbSNPrs527236085
ebirs527236085
HLIrs527236085
Exacrs527236085
Varsomers527236085
Maprs527236085
PheGenIrs527236085
hapmaprs527236085
1000 genomesrs527236085
hgdprs527236085
ensemblrs527236085
gopubmedrs527236085
geneviewrs527236085
scholarrs527236085
googlers527236085
pharmgkbrs527236085
gwascentralrs527236085
openSNPrs527236085
23andMers527236085
23andMe allrs527236085
SNP Nexus

SNPshotrs527236085
SNPdbers527236085
MSV3drs527236085
GWAS Ctlgrs527236085
Max Magnitude0
ClinVar
Risk rs527236085(T;T)
Alt rs527236085(T;T)
Reference rs527236085(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene MYO7A
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000011.9:g.76874011G>T
CLNSRC ClinVar
CLNACC RCV000132570.1,