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rs121909069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909069(C;T)
Make rs121909069(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position3457606
GeneTGIF1
is asnp
is mentioned by
dbSNPrs121909069
ebirs121909069
HLIrs121909069
Exacrs121909069
Varsomers121909069
Maprs121909069
PheGenIrs121909069
hapmaprs121909069
1000 genomesrs121909069
hgdprs121909069
ensemblrs121909069
gopubmedrs121909069
geneviewrs121909069
scholarrs121909069
googlers121909069
pharmgkbrs121909069
gwascentralrs121909069
openSNPrs121909069
23andMers121909069
23andMe allrs121909069
SNP Nexus

SNPshotrs121909069
SNPdbers121909069
MSV3drs121909069
GWAS Ctlgrs121909069
Max Magnitude0
OMIM602630
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909069(T;T)
Alt rs121909069(T;T)
Reference rs121909069(C;C)
Significance Pathogenic
Disease Holoprosencephaly 4
Variation info
Gene TGIF1
CLNDBN Holoprosencephaly 4
Reversed 0
HGVS NC_000018.9:g.3457604C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007397.3,