Rs104894926

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894926(C;G)
Make rs104894926(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position46853826
GeneRP2
is asnp
is mentioned by
dbSNPrs104894926
Exacrs104894926
PheGenIrs104894926
nextbiors104894926
hapmaprs104894926
1000 genomesrs104894926
hgdprs104894926
ensemblrs104894926
gopubmedrs104894926
geneviewrs104894926
scholarrs104894926
googlers104894926
pharmgkbrs104894926
gwascentralrs104894926
openSNPrs104894926
23andMers104894926
23andMe allrs104894926
SNP Nexus

SNPshotrs104894926
SNPdbers104894926
MSV3drs104894926
OMIM300757
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894926(G;G)
Alt rs104894926(G;G)
Reference rs104894926(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 2
Variation info
Gene RP2
CLNDBN Retinitis pigmentosa 2
Reversed 0
HGVS NC_000023.10:g.46713261C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011293.1,