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

rs61748429

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs61748429(-;-)
Make rs61748429(-;TG)
ReferenceGRCh38 38.1/142
Chromosome6
Position42698438
GeneLOC101929618, PRPH2
is asnp
is mentioned by
dbSNPrs61748429
ebirs61748429
HLIrs61748429
Exacrs61748429
Varsomers61748429
Maprs61748429
PheGenIrs61748429
hapmaprs61748429
1000 genomesrs61748429
hgdprs61748429
ensemblrs61748429
gopubmedrs61748429
geneviewrs61748429
scholarrs61748429
googlers61748429
pharmgkbrs61748429
gwascentralrs61748429
openSNPrs61748429
23andMers61748429
23andMe allrs61748429
SNP Nexus

SNPshotrs61748429
SNPdbers61748429
MSV3drs61748429
GWAS Ctlgrs61748429
Max Magnitude0
ClinVar
Risk rs61748429(;)
Alt rs61748429(;)
Reference rs61748429(TG;TG)
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.42666176_42666177delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000014057.25, RCV000085029.1,