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rs796053430

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053430(A;G)
Make rs796053430(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position55229005
GeneTCF4
is asnp
is mentioned by
dbSNPrs796053430
ebirs796053430
HLIrs796053430
Exacrs796053430
Varsomers796053430
Maprs796053430
PheGenIrs796053430
hapmaprs796053430
1000 genomesrs796053430
hgdprs796053430
ensemblrs796053430
gopubmedrs796053430
geneviewrs796053430
scholarrs796053430
googlers796053430
pharmgkbrs796053430
gwascentralrs796053430
openSNPrs796053430
23andMers796053430
23andMe allrs796053430
SNP Nexus

SNPshotrs796053430
SNPdbers796053430
MSV3drs796053430
GWAS Ctlgrs796053430
Max Magnitude0
ClinVar
Risk rs796053430(G;G)
Alt rs796053430(G;G)
Reference rs796053430(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52896236T>C
CLNSRC
CLNACC RCV000189737.1,