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rs1064796853

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position55279554
GeneTCF4
is asnp
is mentioned by
dbSNPrs1064796853
dbSNP (classic)rs1064796853
ClinGenrs1064796853
ebirs1064796853
HLIrs1064796853
Exacrs1064796853
Gnomadrs1064796853
Varsomers1064796853
LitVarrs1064796853
Maprs1064796853
PheGenIrs1064796853
Biobankrs1064796853
1000 genomesrs1064796853
hgdprs1064796853
ensemblrs1064796853
geneviewrs1064796853
scholarrs1064796853
googlers1064796853
pharmgkbrs1064796853
gwascentralrs1064796853
openSNPrs1064796853
23andMers1064796853
23andMe allrs1064796853
SNPshotrs1064796853
SNPdbers1064796853
MSV3drs1064796853
GWAS Ctlgrs1064796853
Max Magnitude0
ClinVar
Risk rs1064796853(T;T)
Alt rs1064796853(T;T)
Reference Rs1064796853(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52946785G>A
CLNSRC
CLNACC RCV000486556.1,