Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853149

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853149(C;T)
Make rs878853149(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position55350388
GeneTCF4
is asnp
is mentioned by
dbSNPrs878853149
ebirs878853149
HLIrs878853149
Exacrs878853149
Varsomers878853149
Maprs878853149
PheGenIrs878853149
hapmaprs878853149
1000 genomesrs878853149
hgdprs878853149
ensemblrs878853149
gopubmedrs878853149
geneviewrs878853149
scholarrs878853149
googlers878853149
pharmgkbrs878853149
gwascentralrs878853149
openSNPrs878853149
23andMers878853149
23andMe allrs878853149
SNP Nexus

SNPshotrs878853149
SNPdbers878853149
MSV3drs878853149
GWAS Ctlgrs878853149
Max Magnitude0
ClinVar
Risk rs878853149(T;T)
Alt rs878853149(T;T)
Reference rs878853149(C;C)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene TCF4
CLNDBN Intellectual disability
Reversed 1
HGVS NC_000018.9:g.53017619G>A
CLNSRC
CLNACC RCV000224478.1,