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rs121909067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909067(C;G)
Make rs121909067(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position3456525
GeneTGIF1
is asnp
is mentioned by
dbSNPrs121909067
ebirs121909067
HLIrs121909067
Exacrs121909067
Varsomers121909067
Maprs121909067
PheGenIrs121909067
hapmaprs121909067
1000 genomesrs121909067
hgdprs121909067
ensemblrs121909067
gopubmedrs121909067
geneviewrs121909067
scholarrs121909067
googlers121909067
pharmgkbrs121909067
gwascentralrs121909067
openSNPrs121909067
23andMers121909067
23andMe allrs121909067
SNP Nexus

SNPshotrs121909067
SNPdbers121909067
MSV3drs121909067
GWAS Ctlgrs121909067
Max Magnitude0
OMIM602630
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909067(G;G)
Alt rs121909067(G;G)
Reference rs121909067(C;C)
Significance Pathogenic
Disease Holoprosencephaly 4
Variation info
Gene TGIF1
CLNDBN Holoprosencephaly 4
Reversed 0
HGVS NC_000018.9:g.3456523C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007395.3,