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rs104894039

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894039(A;G)
Make rs104894039(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position33095391
GeneLOC101928355, RP9
is asnp
is mentioned by
dbSNPrs104894039
ebirs104894039
HLIrs104894039
Exacrs104894039
Varsomers104894039
Maprs104894039
PheGenIrs104894039
hapmaprs104894039
1000 genomesrs104894039
hgdprs104894039
ensemblrs104894039
gopubmedrs104894039
geneviewrs104894039
scholarrs104894039
googlers104894039
pharmgkbrs104894039
gwascentralrs104894039
openSNPrs104894039
23andMers104894039
23andMe allrs104894039
SNP Nexus

SNPshotrs104894039
SNPdbers104894039
MSV3drs104894039
GWAS Ctlgrs104894039
Max Magnitude0
OMIM607331
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894039(G;G)
Alt rs104894039(G;G)
Reference rs104894039(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 9
Variation info
Gene RP9 LOC101928355
CLNDBN Retinitis pigmentosa 9
Reversed 1
HGVS NC_000007.13:g.33135003T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003499.3,