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rs1064796134

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome18
Position55232605
GeneTCF4
is asnp
is mentioned by
dbSNPrs1064796134
dbSNP (old)rs1064796134
ClinGenrs1064796134
ebirs1064796134
HLIrs1064796134
Exacrs1064796134
Gnomadrs1064796134
Varsomers1064796134
Maprs1064796134
PheGenIrs1064796134
Biobankrs1064796134
1000 genomesrs1064796134
hgdprs1064796134
ensemblrs1064796134
gopubmedrs1064796134
geneviewrs1064796134
scholarrs1064796134
googlers1064796134
pharmgkbrs1064796134
gwascentralrs1064796134
openSNPrs1064796134
23andMers1064796134
23andMe allrs1064796134
SNPshotrs1064796134
SNPdbers1064796134
MSV3drs1064796134
GWAS Ctlgrs1064796134
Max Magnitude0
ClinVar
Risk rs1064796134(-;-)
Alt rs1064796134(-;-)
Reference Rs1064796134(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52899836delT
CLNSRC
CLNACC RCV000482160.1,