Rs104894927

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894927(C;T)
Make rs104894927(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position46853731
GeneRP2
is asnp
is mentioned by
dbSNPrs104894927
Exacrs104894927
PheGenIrs104894927
nextbiors104894927
hapmaprs104894927
1000 genomesrs104894927
hgdprs104894927
ensemblrs104894927
gopubmedrs104894927
geneviewrs104894927
scholarrs104894927
googlers104894927
pharmgkbrs104894927
gwascentralrs104894927
openSNPrs104894927
23andMers104894927
23andMe allrs104894927
SNP Nexus

SNPshotrs104894927
SNPdbers104894927
MSV3drs104894927
Max Magnitude0
OMIM300757
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894927(T;T)
Alt rs104894927(T;T)
Reference rs104894927(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 2
Variation info
Gene RP2
CLNDBN Retinitis pigmentosa 2
Reversed 0
HGVS NC_000023.10:g.46713166C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011297.3,