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rs1057517838

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517838(A;A)
Make rs1057517838(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position24256063
GeneTGM1
is asnp
is mentioned by
dbSNPrs1057517838
dbSNP (old)rs1057517838
ClinGenrs1057517838
ebirs1057517838
HLIrs1057517838
Exacrs1057517838
Gnomadrs1057517838
Varsomers1057517838
Maprs1057517838
PheGenIrs1057517838
Biobankrs1057517838
1000 genomesrs1057517838
hgdprs1057517838
ensemblrs1057517838
gopubmedrs1057517838
geneviewrs1057517838
scholarrs1057517838
googlers1057517838
pharmgkbrs1057517838
gwascentralrs1057517838
openSNPrs1057517838
23andMers1057517838
23andMe allrs1057517838
SNPshotrs1057517838
SNPdbers1057517838
MSV3drs1057517838
GWAS Ctlgrs1057517838
Max Magnitude0
ClinVar
Risk rs1057517838(A;A)
Alt rs1057517838(A;A)
Reference Rs1057517838(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TGM1
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.24725269C>T
CLNSRC
CLNACC RCV000413793.1,