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rs1064796538

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position55269880
GeneTCF4
is asnp
is mentioned by
dbSNPrs1064796538
dbSNP (old)rs1064796538
ClinGenrs1064796538
ebirs1064796538
HLIrs1064796538
Exacrs1064796538
Gnomadrs1064796538
Varsomers1064796538
Maprs1064796538
PheGenIrs1064796538
Biobankrs1064796538
1000 genomesrs1064796538
hgdprs1064796538
ensemblrs1064796538
gopubmedrs1064796538
geneviewrs1064796538
scholarrs1064796538
googlers1064796538
pharmgkbrs1064796538
gwascentralrs1064796538
openSNPrs1064796538
23andMers1064796538
23andMe allrs1064796538
SNPshotrs1064796538
SNPdbers1064796538
MSV3drs1064796538
GWAS Ctlgrs1064796538
Max Magnitude0
ClinVar
Risk rs1064796538(G;G)
Alt rs1064796538(G;G)
Reference Rs1064796538(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52937111G>C
CLNSRC
CLNACC RCV000481651.1,