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rs796053428

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053428(-;GGCC)
Make rs796053428(GGCC;GGCC)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position55228271
GeneTCF4
is asnp
is mentioned by
dbSNPrs796053428
ClinGenrs796053428
ebirs796053428
HLIrs796053428
Exacrs796053428
Varsomers796053428
Maprs796053428
PheGenIrs796053428
hapmaprs796053428
1000 genomesrs796053428
hgdprs796053428
ensemblrs796053428
gopubmedrs796053428
geneviewrs796053428
scholarrs796053428
googlers796053428
pharmgkbrs796053428
gwascentralrs796053428
openSNPrs796053428
23andMers796053428
23andMe allrs796053428
SNP Nexus

SNPshotrs796053428
SNPdbers796053428
MSV3drs796053428
GWAS Ctlgrs796053428
Max Magnitude0
ClinVar
Risk rs796053428(GGCC;GGCC)
Alt rs796053428(GGCC;GGCC)
Reference Rs796053428(;)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52895503_52895506dupGGCC
CLNSRC
CLNACC RCV000189733.1,