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rs1057524509

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524509(G;T)
Make rs1057524509(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position57243471
GeneTCF12
is asnp
is mentioned by
dbSNPrs1057524509
dbSNP (old)rs1057524509
ClinGenrs1057524509
ebirs1057524509
HLIrs1057524509
Exacrs1057524509
Gnomadrs1057524509
Varsomers1057524509
LitVarrs1057524509
Maprs1057524509
PheGenIrs1057524509
Biobankrs1057524509
1000 genomesrs1057524509
hgdprs1057524509
ensemblrs1057524509
gopubmedrs1057524509
geneviewrs1057524509
scholarrs1057524509
googlers1057524509
pharmgkbrs1057524509
gwascentralrs1057524509
openSNPrs1057524509
23andMers1057524509
23andMe allrs1057524509
SNPshotrs1057524509
SNPdbers1057524509
MSV3drs1057524509
GWAS Ctlgrs1057524509
Max Magnitude0
ClinVar
Risk rs1057524509(T;T)
Alt rs1057524509(T;T)
Reference Rs1057524509(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCF12
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.57535669G>T
CLNSRC
CLNACC RCV000419466.1,