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

rs61755777

From SNPedia

Orientationminus
Make rs61755777(-;-)
Make rs61755777(-;TGC)
Make rs61755777(TGC;TGC)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position42721978
GenePRPH2
is asnp
is mentioned by
dbSNPrs61755777
ebirs61755777
HLIrs61755777
Exacrs61755777
Varsomers61755777
Maprs61755777
PheGenIrs61755777
hapmaprs61755777
1000 genomesrs61755777
hgdprs61755777
ensemblrs61755777
gopubmedrs61755777
geneviewrs61755777
scholarrs61755777
googlers61755777
pharmgkbrs61755777
gwascentralrs61755777
openSNPrs61755777
23andMers61755777
23andMe allrs61755777
SNP Nexus

SNPshotrs61755777
SNPdbers61755777
MSV3drs61755777
GWAS Ctlgrs61755777
Max Magnitude
ClinVar
Risk rs61755777(;)
Alt rs61755777(;)
Reference rs61755777(GCT;GCT)
Significance Pathogenic
Disease Retinitis pigmentosa 7 not provided
Variation info
Gene PRPH2
CLNDBN Retinitis pigmentosa 7 not provided
Reversed 1
HGVS NC_000006.11:g.42689715_42689717delAGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000014048.24, RCV000084963.1,