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

rs61755789

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61755789(A;A)
Make rs61755789(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position42721835
GenePRPH2
is asnp
is mentioned by
dbSNPrs61755789
ebirs61755789
HLIrs61755789
Exacrs61755789
Varsomers61755789
Maprs61755789
PheGenIrs61755789
hapmaprs61755789
1000 genomesrs61755789
hgdprs61755789
ensemblrs61755789
gopubmedrs61755789
geneviewrs61755789
scholarrs61755789
googlers61755789
pharmgkbrs61755789
gwascentralrs61755789
openSNPrs61755789
23andMers61755789
23andMe allrs61755789
SNP Nexus

SNPshotrs61755789
SNPdbers61755789
MSV3drs61755789
GWAS Ctlgrs61755789
Max Magnitude0
OMIM179605
Desc
Variant0009
Relatedalso


ClinVar
Risk rs61755789(A;A)
Alt rs61755789(A;A)
Reference rs61755789(G;G)
Significance Pathogenic
Disease Patterned dystrophy of retinal pigment epithelium not provided
Variation info
Gene PRPH2
CLNDBN Patterned dystrophy of retinal pigment epithelium not provided
Reversed 1
HGVS NC_000006.11:g.42689573C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014055.25, RCV000084977.1,