Rs104894187

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Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894187(A;C)
Make rs104894187(C;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position84247707
GeneRGR
is asnp
is mentioned by
dbSNPrs104894187
Exacrs104894187
PheGenIrs104894187
nextbiors104894187
hapmaprs104894187
1000 genomesrs104894187
hgdprs104894187
ensemblrs104894187
gopubmedrs104894187
geneviewrs104894187
scholarrs104894187
googlers104894187
pharmgkbrs104894187
gwascentralrs104894187
openSNPrs104894187
23andMers104894187
23andMe allrs104894187
SNP Nexus

SNPshotrs104894187
SNPdbers104894187
MSV3drs104894187
OMIM600342
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894187(C;C)
Alt rs104894187(C;C)
Reference rs104894187(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 44
Variation info
Gene RGR
CLNDBN Retinitis pigmentosa 44
Reversed 0
HGVS NC_000010.10:g.86007463A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009759.2,