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rs1057517837

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517837(C;C)
Make rs1057517837(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position24259152
GeneTGM1
is asnp
is mentioned by
dbSNPrs1057517837
dbSNP (old)rs1057517837
ClinGenrs1057517837
ebirs1057517837
HLIrs1057517837
Exacrs1057517837
Gnomadrs1057517837
Varsomers1057517837
LitVarrs1057517837
Maprs1057517837
PheGenIrs1057517837
Biobankrs1057517837
1000 genomesrs1057517837
hgdprs1057517837
ensemblrs1057517837
gopubmedrs1057517837
geneviewrs1057517837
scholarrs1057517837
googlers1057517837
pharmgkbrs1057517837
gwascentralrs1057517837
openSNPrs1057517837
23andMers1057517837
23andMe allrs1057517837
SNPshotrs1057517837
SNPdbers1057517837
MSV3drs1057517837
GWAS Ctlgrs1057517837
Max Magnitude0
ClinVar
Risk rs1057517837(C;C)
Alt rs1057517837(C;C)
Reference Rs1057517837(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene TGM1
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.24728358A>G
CLNSRC
CLNACC RCV000414543.1,