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

rs796053418

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053418(C;T)
Make rs796053418(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position55232588
GeneTCF4
is asnp
is mentioned by
dbSNPrs796053418
ebirs796053418
HLIrs796053418
Exacrs796053418
Varsomers796053418
Maprs796053418
PheGenIrs796053418
hapmaprs796053418
1000 genomesrs796053418
hgdprs796053418
ensemblrs796053418
gopubmedrs796053418
geneviewrs796053418
scholarrs796053418
googlers796053418
pharmgkbrs796053418
gwascentralrs796053418
openSNPrs796053418
23andMers796053418
23andMe allrs796053418
SNP Nexus

SNPshotrs796053418
SNPdbers796053418
MSV3drs796053418
GWAS Ctlgrs796053418
Max Magnitude0
ClinVar
Risk rs796053418(T;T)
Alt rs796053418(T;T)
Reference rs796053418(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52899819G>A
CLNSRC
CLNACC RCV000189722.1,