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rs61755816

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61755816(A;A)
Make rs61755816(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position42704461
GeneLOC101929618, PRPH2
is asnp
is mentioned by
dbSNPrs61755816
ebirs61755816
HLIrs61755816
Exacrs61755816
Varsomers61755816
Maprs61755816
PheGenIrs61755816
hapmaprs61755816
1000 genomesrs61755816
hgdprs61755816
ensemblrs61755816
gopubmedrs61755816
geneviewrs61755816
scholarrs61755816
googlers61755816
pharmgkbrs61755816
gwascentralrs61755816
openSNPrs61755816
23andMers61755816
23andMe allrs61755816
SNP Nexus

SNPshotrs61755816
SNPdbers61755816
MSV3drs61755816
GWAS Ctlgrs61755816
Max Magnitude0
OMIM179605
Desc
Variant0011
Relatedalso


ClinVar
Risk rs61755816(A,G;A,G)
Alt rs61755816(A,G;A,G)
Reference rs61755816(C;C)
Significance Pathogenic
Disease not provided Retinitis pigmentosa 7
Variation info
Gene PRPH2
CLNDBN not provided Retinitis pigmentosa 7
Reversed 1
HGVS NC_000006.11:g.42672199G>C; NC_000006.11:g.42672199G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000085018.1, RCV000014058.18, RCV000085017.1,