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rs796053424

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053424(-;AG)
Make rs796053424(AG;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position55350390
GeneTCF4
is asnp
is mentioned by
dbSNPrs796053424
ClinGenrs796053424
ebirs796053424
HLIrs796053424
Exacrs796053424
Varsomers796053424
Maprs796053424
PheGenIrs796053424
hapmaprs796053424
1000 genomesrs796053424
hgdprs796053424
ensemblrs796053424
gopubmedrs796053424
geneviewrs796053424
scholarrs796053424
googlers796053424
pharmgkbrs796053424
gwascentralrs796053424
openSNPrs796053424
23andMers796053424
23andMe allrs796053424
SNP Nexus

SNPshotrs796053424
SNPdbers796053424
MSV3drs796053424
GWAS Ctlgrs796053424
Max Magnitude0
ClinVar
Risk rs796053424(AG;AG)
Alt rs796053424(AG;AG)
Reference Rs796053424(;)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.53017622_53017623dupCT
CLNSRC
CLNACC RCV000189729.1,