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rs61755769

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs61755769(-;-)
Make rs61755769(-;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position42722222
GenePRPH2
is asnp
is mentioned by
dbSNPrs61755769
ebirs61755769
HLIrs61755769
Exacrs61755769
Varsomers61755769
Maprs61755769
PheGenIrs61755769
hapmaprs61755769
1000 genomesrs61755769
hgdprs61755769
ensemblrs61755769
gopubmedrs61755769
geneviewrs61755769
scholarrs61755769
googlers61755769
pharmgkbrs61755769
gwascentralrs61755769
openSNPrs61755769
23andMers61755769
23andMe allrs61755769
SNP Nexus

SNPshotrs61755769
SNPdbers61755769
MSV3drs61755769
GWAS Ctlgrs61755769
Max Magnitude0
ClinVar
Risk rs61755769(;)
Alt rs61755769(;)
Reference rs61755769(G;G)
Significance Pathogenic
Disease Macular dystrophy not provided
Variation info
Gene PRPH2
CLNDBN Macular dystrophy, vitelliform, adult-onset not provided
Reversed 1
HGVS NC_000006.11:g.42689960delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000014063.27, RCV000084953.1,