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rs61755806

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61755806(C;T)
Make rs61755806(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position42704546
GeneLOC101929618, PRPH2
is asnp
is mentioned by
dbSNPrs61755806
ebirs61755806
HLIrs61755806
Exacrs61755806
Varsomers61755806
Maprs61755806
PheGenIrs61755806
hapmaprs61755806
1000 genomesrs61755806
hgdprs61755806
ensemblrs61755806
gopubmedrs61755806
geneviewrs61755806
scholarrs61755806
googlers61755806
pharmgkbrs61755806
gwascentralrs61755806
openSNPrs61755806
23andMers61755806
23andMe allrs61755806
SNP Nexus

SNPshotrs61755806
SNPdbers61755806
MSV3drs61755806
GWAS Ctlgrs61755806
Max Magnitude0
OMIM179605
Desc
Variant0003
Relatedalso


ClinVar
Risk rs61755806(T;T)
Alt rs61755806(T;T)
Reference rs61755806(C;C)
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.42672284G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014050.25, RCV000085007.1,