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rs121909075

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909075(A;A)
Make rs121909075(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position35500100
GeneTULP1
is asnp
is mentioned by
dbSNPrs121909075
ebirs121909075
HLIrs121909075
Exacrs121909075
Varsomers121909075
Maprs121909075
PheGenIrs121909075
hapmaprs121909075
1000 genomesrs121909075
hgdprs121909075
ensemblrs121909075
gopubmedrs121909075
geneviewrs121909075
scholarrs121909075
googlers121909075
pharmgkbrs121909075
gwascentralrs121909075
openSNPrs121909075
23andMers121909075
23andMe allrs121909075
SNP Nexus

SNPshotrs121909075
SNPdbers121909075
MSV3drs121909075
GWAS Ctlgrs121909075
GMAF0.0004591
Max Magnitude0
OMIM602280
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909075(A,C;A,C)
Alt rs121909075(A,C;A,C)
Reference rs121909075(T;T)
Significance Pathogenic
Disease not provided Retinitis pigmentosa 14
Variation info
Gene TULP1
CLNDBN not provided Retinitis pigmentosa 14
Reversed 1
HGVS NC_000006.11:g.35467877A>G; NC_000006.11:g.35467877A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000174738.1, RCV000007784.3,