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rs61755807

From SNPedia

Orientationminus
Make rs61755807(-;-)
Make rs61755807(-;CAC)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position42704535
GenePRPH2
is asnp
is mentioned by
dbSNPrs61755807
ebirs61755807
HLIrs61755807
Exacrs61755807
Varsomers61755807
Maprs61755807
PheGenIrs61755807
hapmaprs61755807
1000 genomesrs61755807
hgdprs61755807
ensemblrs61755807
gopubmedrs61755807
geneviewrs61755807
scholarrs61755807
googlers61755807
pharmgkbrs61755807
gwascentralrs61755807
openSNPrs61755807
23andMers61755807
23andMe allrs61755807
SNP Nexus

SNPshotrs61755807
SNPdbers61755807
MSV3drs61755807
GWAS Ctlgrs61755807
Max Magnitude
ClinVar
Risk rs61755807(;)
Alt rs61755807(;)
Reference rs61755807(CAC;CAC)
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.42672273_42672275delGTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000014049.18, RCV000085009.1,