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rs878853094

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853094(A;A)
Make rs878853094(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position57234112
GeneTCF12
is asnp
is mentioned by
dbSNPrs878853094
ebirs878853094
HLIrs878853094
Exacrs878853094
Varsomers878853094
Maprs878853094
PheGenIrs878853094
hapmaprs878853094
1000 genomesrs878853094
hgdprs878853094
ensemblrs878853094
gopubmedrs878853094
geneviewrs878853094
scholarrs878853094
googlers878853094
pharmgkbrs878853094
gwascentralrs878853094
openSNPrs878853094
23andMers878853094
23andMe allrs878853094
SNP Nexus

SNPshotrs878853094
SNPdbers878853094
MSV3drs878853094
GWAS Ctlgrs878853094
Max Magnitude0
ClinVar
Risk rs878853094(A;A)
Alt rs878853094(A;A)
Reference rs878853094(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TCF12
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.57526310G>A
CLNSRC
CLNACC RCV000224406.1,