Rs104894925

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894925(C;T)
Make rs104894925(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position46837176
GeneRP2
is asnp
is mentioned by
dbSNPrs104894925
Exacrs104894925
PheGenIrs104894925
nextbiors104894925
hapmaprs104894925
1000 genomesrs104894925
hgdprs104894925
ensemblrs104894925
gopubmedrs104894925
geneviewrs104894925
scholarrs104894925
googlers104894925
pharmgkbrs104894925
gwascentralrs104894925
openSNPrs104894925
23andMers104894925
23andMe allrs104894925
SNP Nexus

SNPshotrs104894925
SNPdbers104894925
MSV3drs104894925
Max Magnitude0
OMIM300757
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894925(T;T)
Alt rs104894925(T;T)
Reference rs104894925(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 2
Variation info
Gene RP2
CLNDBN Retinitis pigmentosa 2
Reversed 0
HGVS NC_000023.10:g.46696611C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011291.4,