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rs796053420

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053420(C;G)
Make rs796053420(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position55232524
GeneTCF4
is asnp
is mentioned by
dbSNPrs796053420
ClinGenrs796053420
ebirs796053420
HLIrs796053420
Exacrs796053420
Varsomers796053420
Maprs796053420
PheGenIrs796053420
hapmaprs796053420
1000 genomesrs796053420
hgdprs796053420
ensemblrs796053420
gopubmedrs796053420
geneviewrs796053420
scholarrs796053420
googlers796053420
pharmgkbrs796053420
gwascentralrs796053420
openSNPrs796053420
23andMers796053420
23andMe allrs796053420
SNP Nexus

SNPshotrs796053420
SNPdbers796053420
MSV3drs796053420
GWAS Ctlgrs796053420
Max Magnitude0
ClinVar
Risk rs796053420(G;G)
Alt rs796053420(G;G)
Reference Rs796053420(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52899755G>C
CLNSRC
CLNACC RCV000189724.1,