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rs142634031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs142634031(C;C)
Make rs142634031(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome14
Position24259813
GeneTGM1
is asnp
is mentioned by
dbSNPrs142634031
dbSNP (classic)rs142634031
ClinGenrs142634031
ebirs142634031
HLIrs142634031
Exacrs142634031
Gnomadrs142634031
Varsomers142634031
LitVarrs142634031
Maprs142634031
PheGenIrs142634031
Biobankrs142634031
1000 genomesrs142634031
hgdprs142634031
ensemblrs142634031
geneviewrs142634031
scholarrs142634031
googlers142634031
pharmgkbrs142634031
gwascentralrs142634031
openSNPrs142634031
23andMers142634031
23andMe allrs142634031
SNPshotrs142634031
SNPdbers142634031
MSV3drs142634031
GWAS Ctlgrs142634031
Max Magnitude0
ClinVar
Risk rs142634031(C;C)
Alt rs142634031(C;C)
Reference Rs142634031(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TGM1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.24729019T>C
CLNSRC
CLNACC RCV000290112.1,