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rs796053429

From SNPedia

Orientationminus
Make rs796053429(-;-)
Make rs796053429(-;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position55228230
GeneTCF4
is asnp
is mentioned by
dbSNPrs796053429
ebirs796053429
HLIrs796053429
Exacrs796053429
Varsomers796053429
Maprs796053429
PheGenIrs796053429
hapmaprs796053429
1000 genomesrs796053429
hgdprs796053429
ensemblrs796053429
gopubmedrs796053429
geneviewrs796053429
scholarrs796053429
googlers796053429
pharmgkbrs796053429
gwascentralrs796053429
openSNPrs796053429
23andMers796053429
23andMe allrs796053429
SNP Nexus

SNPshotrs796053429
SNPdbers796053429
MSV3drs796053429
GWAS Ctlgrs796053429
Max Magnitude
ClinVar
Risk rs796053429(;)
Alt rs796053429(;)
Reference rs796053429(GA;GA)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52895461_52895462delTC
CLNSRC
CLNACC RCV000189734.1,