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rs121909074

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909074(C;C)
Make rs121909074(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position35500005
GeneTULP1
is asnp
is mentioned by
dbSNPrs121909074
ebirs121909074
HLIrs121909074
Exacrs121909074
Varsomers121909074
Maprs121909074
PheGenIrs121909074
hapmaprs121909074
1000 genomesrs121909074
hgdprs121909074
ensemblrs121909074
gopubmedrs121909074
geneviewrs121909074
scholarrs121909074
googlers121909074
pharmgkbrs121909074
gwascentralrs121909074
openSNPrs121909074
23andMers121909074
23andMe allrs121909074
SNP Nexus

SNPshotrs121909074
SNPdbers121909074
MSV3drs121909074
GWAS Ctlgrs121909074
Max Magnitude0
OMIM602280
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909074(C;C)
Alt rs121909074(C;C)
Reference rs121909074(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 14
Variation info
Gene TULP1
CLNDBN Retinitis pigmentosa 14
Reversed 1
HGVS NC_000006.11:g.35467782A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007783.3,