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rs104894037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894037(A;T)
Make rs104894037(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position33096550
GeneRP9
is asnp
is mentioned by
dbSNPrs104894037
ebirs104894037
HLIrs104894037
Exacrs104894037
Varsomers104894037
Maprs104894037
PheGenIrs104894037
hapmaprs104894037
1000 genomesrs104894037
hgdprs104894037
ensemblrs104894037
gopubmedrs104894037
geneviewrs104894037
scholarrs104894037
googlers104894037
pharmgkbrs104894037
gwascentralrs104894037
openSNPrs104894037
23andMers104894037
23andMe allrs104894037
SNP Nexus

SNPshotrs104894037
SNPdbers104894037
MSV3drs104894037
GWAS Ctlgrs104894037
Max Magnitude0
OMIM607331
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894037(T;T)
Alt rs104894037(T;T)
Reference rs104894037(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 9
Variation info
Gene RP9
CLNDBN Retinitis pigmentosa 9
Reversed 1
HGVS NC_000007.13:g.33136162T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003498.3,