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rs796053425

From SNPedia

Orientationminus
Make rs796053425(GGA;T)
Make rs796053425(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position55275726
GeneTCF4
is asnp
is mentioned by
dbSNPrs796053425
ebirs796053425
HLIrs796053425
Exacrs796053425
Varsomers796053425
Maprs796053425
PheGenIrs796053425
hapmaprs796053425
1000 genomesrs796053425
hgdprs796053425
ensemblrs796053425
gopubmedrs796053425
geneviewrs796053425
scholarrs796053425
googlers796053425
pharmgkbrs796053425
gwascentralrs796053425
openSNPrs796053425
23andMers796053425
23andMe allrs796053425
SNP Nexus

SNPshotrs796053425
SNPdbers796053425
MSV3drs796053425
GWAS Ctlgrs796053425
Max Magnitude
ClinVar
Risk rs796053425(T;T)
Alt rs796053425(T;T)
Reference rs796053425(GGA;GGA)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52942957_52942959delTCCinsA
CLNSRC
CLNACC RCV000189730.1,