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rs61755781

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61755781(A;G)
Make rs61755781(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position42721913
GenePRPH2
is asnp
is mentioned by
dbSNPrs61755781
ebirs61755781
HLIrs61755781
Exacrs61755781
Varsomers61755781
Maprs61755781
PheGenIrs61755781
hapmaprs61755781
1000 genomesrs61755781
hgdprs61755781
ensemblrs61755781
gopubmedrs61755781
geneviewrs61755781
scholarrs61755781
googlers61755781
pharmgkbrs61755781
gwascentralrs61755781
openSNPrs61755781
23andMers61755781
23andMe allrs61755781
SNP Nexus

SNPshotrs61755781
SNPdbers61755781
MSV3drs61755781
GWAS Ctlgrs61755781
Max Magnitude0
ClinVar
Risk rs61755781(G;G)
Alt rs61755781(G;G)
Reference rs61755781(A;A)
Significance Pathogenic
Disease not provided Macular dystrophy Patterned dystrophy of retinal pigment epithelium
Variation info
Gene PRPH2
CLNDBN not provided Macular dystrophy, vitelliform, adult-onset Patterned dystrophy of retinal pigment epithelium
Reversed 1
HGVS NC_000006.11:g.42689651T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000084969.1, RCV000161144.3, RCV000161145.3,