Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057524821

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524821(C;C)
Make rs1057524821(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position55228900
GeneTCF4
is asnp
is mentioned by
dbSNPrs1057524821
dbSNP (classic)rs1057524821
ClinGenrs1057524821
ebirs1057524821
HLIrs1057524821
Exacrs1057524821
Gnomadrs1057524821
Varsomers1057524821
LitVarrs1057524821
Maprs1057524821
PheGenIrs1057524821
Biobankrs1057524821
1000 genomesrs1057524821
hgdprs1057524821
ensemblrs1057524821
geneviewrs1057524821
scholarrs1057524821
googlers1057524821
pharmgkbrs1057524821
gwascentralrs1057524821
openSNPrs1057524821
23andMers1057524821
23andMe allrs1057524821
SNPshotrs1057524821
SNPdbers1057524821
MSV3drs1057524821
GWAS Ctlgrs1057524821
Max Magnitude0
ClinVar
Risk rs1057524821(C;C)
Alt rs1057524821(C;C)
Reference Rs1057524821(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52896131A>G
CLNSRC
CLNACC RCV000418798.1,