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rs1064795443

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position55229010
GeneTCF4
is asnp
is mentioned by
dbSNPrs1064795443
dbSNP (old)rs1064795443
ClinGenrs1064795443
ebirs1064795443
HLIrs1064795443
Exacrs1064795443
Gnomadrs1064795443
Varsomers1064795443
Maprs1064795443
PheGenIrs1064795443
Biobankrs1064795443
1000 genomesrs1064795443
hgdprs1064795443
ensemblrs1064795443
gopubmedrs1064795443
geneviewrs1064795443
scholarrs1064795443
googlers1064795443
pharmgkbrs1064795443
gwascentralrs1064795443
openSNPrs1064795443
23andMers1064795443
23andMe allrs1064795443
SNPshotrs1064795443
SNPdbers1064795443
MSV3drs1064795443
GWAS Ctlgrs1064795443
Max Magnitude0
ClinVar
Risk rs1064795443(-;-)
Alt rs1064795443(-;-)
Reference Rs1064795443(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52896241delG
CLNSRC
CLNACC RCV000485949.1,