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rs61755798

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61755798(C;G)
Make rs61755798(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position42704564
GeneLOC101929618, PRPH2
is asnp
is mentioned by
dbSNPrs61755798
ebirs61755798
HLIrs61755798
Exacrs61755798
Varsomers61755798
Maprs61755798
PheGenIrs61755798
hapmaprs61755798
1000 genomesrs61755798
hgdprs61755798
ensemblrs61755798
gopubmedrs61755798
geneviewrs61755798
scholarrs61755798
googlers61755798
pharmgkbrs61755798
gwascentralrs61755798
openSNPrs61755798
23andMers61755798
23andMe allrs61755798
SNP Nexus

SNPshotrs61755798
SNPdbers61755798
MSV3drs61755798
GWAS Ctlgrs61755798
Max Magnitude0
OMIM179605
Desc
Variant0012
Relatedalso
ClinVar
Risk rs61755798(G,T;G,T)
Alt rs61755798(G,T;G,T)
Reference rs61755798(C;C)
Significance Pathogenic
Disease not provided Macular dystrophy
Variation info
Gene PRPH2
CLNDBN not provided Macular dystrophy, vitelliform, adult-onset
Reversed 1
HGVS NC_000006.11:g.42672302G>A; NC_000006.11:g.42672302G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000084998.1, RCV000014059.26, RCV000084997.1,