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rs121909077

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909077(C;T)
Make rs121909077(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position35500032
GeneTULP1
is asnp
is mentioned by
dbSNPrs121909077
ebirs121909077
HLIrs121909077
Exacrs121909077
Varsomers121909077
Maprs121909077
PheGenIrs121909077
hapmaprs121909077
1000 genomesrs121909077
hgdprs121909077
ensemblrs121909077
gopubmedrs121909077
geneviewrs121909077
scholarrs121909077
googlers121909077
pharmgkbrs121909077
gwascentralrs121909077
openSNPrs121909077
23andMers121909077
23andMe allrs121909077
SNP Nexus

SNPshotrs121909077
SNPdbers121909077
MSV3drs121909077
GWAS Ctlgrs121909077
Max Magnitude0
OMIM602280
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909077(T;T)
Alt rs121909077(T;T)
Reference rs121909077(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 14
Variation info
Gene TULP1
CLNDBN Retinitis pigmentosa 14
Reversed 1
HGVS NC_000006.11:g.35467809G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007788.3,