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rs121909070

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909070(C;G)
Make rs121909070(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position3452156
GeneTGIF1
is asnp
is mentioned by
dbSNPrs121909070
ebirs121909070
HLIrs121909070
Exacrs121909070
Varsomers121909070
Maprs121909070
PheGenIrs121909070
hapmaprs121909070
1000 genomesrs121909070
hgdprs121909070
ensemblrs121909070
gopubmedrs121909070
geneviewrs121909070
scholarrs121909070
googlers121909070
pharmgkbrs121909070
gwascentralrs121909070
openSNPrs121909070
23andMers121909070
23andMe allrs121909070
SNP Nexus

SNPshotrs121909070
SNPdbers121909070
MSV3drs121909070
GWAS Ctlgrs121909070
Max Magnitude0
OMIM602630
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909070(G;G)
Alt rs121909070(G;G)
Reference rs121909070(C;C)
Significance Pathogenic
Disease Holoprosencephaly 4
Variation info
Gene TGIF1
CLNDBN Holoprosencephaly 4
Reversed 0
HGVS NC_000018.9:g.3452154C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007398.3,