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rs121909121

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909121(A;A)
Make rs121909121(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position55228987
GeneTCF4
is asnp
is mentioned by
dbSNPrs121909121
ebirs121909121
HLIrs121909121
Exacrs121909121
Varsomers121909121
Maprs121909121
PheGenIrs121909121
hapmaprs121909121
1000 genomesrs121909121
hgdprs121909121
ensemblrs121909121
gopubmedrs121909121
geneviewrs121909121
scholarrs121909121
googlers121909121
pharmgkbrs121909121
gwascentralrs121909121
openSNPrs121909121
23andMers121909121
23andMe allrs121909121
SNP Nexus

SNPshotrs121909121
SNPdbers121909121
MSV3drs121909121
GWAS Ctlgrs121909121
Max Magnitude0
OMIM602272
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909121(A;A)
Alt rs121909121(A;A)
Reference rs121909121(G;G)
Significance Pathogenic
Disease Pitt-Hopkins syndrome not provided
Variation info
Gene TCF4
CLNDBN Pitt-Hopkins syndrome not provided
Reversed 1
HGVS NC_000018.9:g.52896218C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007796.3, RCV000189725.2,