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rs1057521151

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521151(A;C)
Make rs1057521151(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position119101655
GeneDPAGT1, LOC107984397
is asnp
is mentioned by
dbSNPrs1057521151
dbSNP (old)rs1057521151
ClinGenrs1057521151
ebirs1057521151
HLIrs1057521151
Exacrs1057521151
Gnomadrs1057521151
Varsomers1057521151
LitVarrs1057521151
Maprs1057521151
PheGenIrs1057521151
Biobankrs1057521151
1000 genomesrs1057521151
hgdprs1057521151
ensemblrs1057521151
gopubmedrs1057521151
geneviewrs1057521151
scholarrs1057521151
googlers1057521151
pharmgkbrs1057521151
gwascentralrs1057521151
openSNPrs1057521151
23andMers1057521151
23andMe allrs1057521151
SNPshotrs1057521151
SNPdbers1057521151
MSV3drs1057521151
GWAS Ctlgrs1057521151
Max Magnitude0
ClinVar
Risk rs1057521151(C;C)
Alt rs1057521151(C;C)
Reference Rs1057521151(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DPAGT1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.118972365T>G
CLNSRC
CLNACC RCV000438342.1,