Have questions? Visit https://www.reddit.com/r/SNPedia

rs61755793

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61755793(A;A)
Make rs61755793(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position42721820
GenePRPH2
is asnp
is mentioned by
dbSNPrs61755793
ebirs61755793
HLIrs61755793
Exacrs61755793
Varsomers61755793
Maprs61755793
PheGenIrs61755793
hapmaprs61755793
1000 genomesrs61755793
hgdprs61755793
ensemblrs61755793
gopubmedrs61755793
geneviewrs61755793
scholarrs61755793
googlers61755793
pharmgkbrs61755793
gwascentralrs61755793
openSNPrs61755793
23andMers61755793
23andMe allrs61755793
SNP Nexus

SNPshotrs61755793
SNPdbers61755793
MSV3drs61755793
GWAS Ctlgrs61755793
Max Magnitude0
OMIM179605
Desc
Variant0006
Relatedalso


ClinVar
Risk rs61755793(A;A)
Alt rs61755793(A;A)
Reference rs61755793(G;G)
Significance Pathogenic
Disease Choroidal dystrophy not provided
Variation info
Gene PRPH2
CLNDBN Choroidal dystrophy, central areolar 2 not provided
Reversed 1
HGVS NC_000006.11:g.42689558C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014053.19, RCV000084982.1,