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rs121909073

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909073(C;C)
Make rs121909073(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position35503623
GeneTULP1
is asnp
is mentioned by
dbSNPrs121909073
ebirs121909073
HLIrs121909073
Exacrs121909073
Varsomers121909073
Maprs121909073
PheGenIrs121909073
hapmaprs121909073
1000 genomesrs121909073
hgdprs121909073
ensemblrs121909073
gopubmedrs121909073
geneviewrs121909073
scholarrs121909073
googlers121909073
pharmgkbrs121909073
gwascentralrs121909073
openSNPrs121909073
23andMers121909073
23andMe allrs121909073
SNP Nexus

SNPshotrs121909073
SNPdbers121909073
MSV3drs121909073
GWAS Ctlgrs121909073
Max Magnitude0
OMIM602280
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909073(C;C)
Alt rs121909073(C;C)
Reference rs121909073(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 14 not provided
Variation info
Gene TULP1
CLNDBN Retinitis pigmentosa 14 not provided
Reversed 1
HGVS NC_000006.11:g.35471400C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007782.4, RCV000086066.1,