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rs104894082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894082(C;T)
Make rs104894082(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position54625911
GeneRP1
is asnp
is mentioned by
dbSNPrs104894082
ebirs104894082
HLIrs104894082
Exacrs104894082
Varsomers104894082
Maprs104894082
PheGenIrs104894082
hapmaprs104894082
1000 genomesrs104894082
hgdprs104894082
ensemblrs104894082
gopubmedrs104894082
geneviewrs104894082
scholarrs104894082
googlers104894082
pharmgkbrs104894082
gwascentralrs104894082
openSNPrs104894082
23andMers104894082
23andMe allrs104894082
SNP Nexus

SNPshotrs104894082
SNPdbers104894082
MSV3drs104894082
GWAS Ctlgrs104894082
Max Magnitude0
OMIM603937
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894082(T;T)
Alt rs104894082(T;T)
Reference rs104894082(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 1
Variation info
Gene RP1
CLNDBN Retinitis pigmentosa 1
Reversed 0
HGVS NC_000008.10:g.55538471C>T
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000006329.5,