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rs121909066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909066(C;G)
Make rs121909066(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position3456420
GeneTGIF1
is asnp
is mentioned by
dbSNPrs121909066
ebirs121909066
HLIrs121909066
Exacrs121909066
Varsomers121909066
Maprs121909066
PheGenIrs121909066
hapmaprs121909066
1000 genomesrs121909066
hgdprs121909066
ensemblrs121909066
gopubmedrs121909066
geneviewrs121909066
scholarrs121909066
googlers121909066
pharmgkbrs121909066
gwascentralrs121909066
openSNPrs121909066
23andMers121909066
23andMe allrs121909066
SNP Nexus

SNPshotrs121909066
SNPdbers121909066
MSV3drs121909066
GWAS Ctlgrs121909066
Max Magnitude0
OMIM602630
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909066(G;G)
Alt rs121909066(G;G)
Reference rs121909066(C;C)
Significance Pathogenic
Disease Holoprosencephaly 4
Variation info
Gene TGIF1
CLNDBN Holoprosencephaly 4
Reversed 0
HGVS NC_000018.9:g.3456418C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007394.3,