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rs1057520132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057520132(-;CT)
Make rs1057520132(CT;CT)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position57262113
GeneTCF12
is asnp
is mentioned by
dbSNPrs1057520132
dbSNP (old)rs1057520132
ClinGenrs1057520132
ebirs1057520132
HLIrs1057520132
Exacrs1057520132
Gnomadrs1057520132
Varsomers1057520132
Maprs1057520132
PheGenIrs1057520132
Biobankrs1057520132
1000 genomesrs1057520132
hgdprs1057520132
ensemblrs1057520132
gopubmedrs1057520132
geneviewrs1057520132
scholarrs1057520132
googlers1057520132
pharmgkbrs1057520132
gwascentralrs1057520132
openSNPrs1057520132
23andMers1057520132
23andMe allrs1057520132
SNPshotrs1057520132
SNPdbers1057520132
MSV3drs1057520132
GWAS Ctlgrs1057520132
Max Magnitude0
ClinVar
Risk rs1057520132(CT;CT)
Alt rs1057520132(CT;CT)
Reference Rs1057520132(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF12
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.57554311_57554312insCT
CLNSRC
CLNACC RCV000440265.1,