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rs121918562

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAC;CAC) 0 common in clinvar
Make rs121918562(-;-)
Make rs121918562(-;CCA)
Make rs121918562(CCA;CCA)
ReferenceGRCh38 38.1/141
Chromosome6
Position42704536
GeneLOC101929618, PRPH2
is asnp
is mentioned by
dbSNPrs121918562
ebirs121918562
HLIrs121918562
Exacrs121918562
Varsomers121918562
Maprs121918562
PheGenIrs121918562
hapmaprs121918562
1000 genomesrs121918562
hgdprs121918562
ensemblrs121918562
gopubmedrs121918562
geneviewrs121918562
scholarrs121918562
googlers121918562
pharmgkbrs121918562
gwascentralrs121918562
openSNPrs121918562
23andMers121918562
23andMe allrs121918562
SNP Nexus

SNPshotrs121918562
SNPdbers121918562
MSV3drs121918562
GWAS Ctlgrs121918562
Max Magnitude0
OMIM179605
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918562(;)
Alt rs121918562(;)
Reference rs121918562(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,