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rs1057521070

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521070(A;A)
Make rs1057521070(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position55228999
GeneTCF4
is asnp
is mentioned by
dbSNPrs1057521070
dbSNP (old)rs1057521070
ClinGenrs1057521070
ebirs1057521070
HLIrs1057521070
Exacrs1057521070
Gnomadrs1057521070
Varsomers1057521070
Maprs1057521070
PheGenIrs1057521070
Biobankrs1057521070
1000 genomesrs1057521070
hgdprs1057521070
ensemblrs1057521070
gopubmedrs1057521070
geneviewrs1057521070
scholarrs1057521070
googlers1057521070
pharmgkbrs1057521070
gwascentralrs1057521070
openSNPrs1057521070
23andMers1057521070
23andMe allrs1057521070
SNPshotrs1057521070
SNPdbers1057521070
MSV3drs1057521070
GWAS Ctlgrs1057521070
Max Magnitude0
ClinVar
Risk rs1057521070(A;A)
Alt rs1057521070(A;A)
Reference Rs1057521070(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52896230C>T
CLNSRC
CLNACC RCV000431775.1,