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rs1057524251

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524251(C;C)
Make rs1057524251(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position146086785
GenePLOD2
is asnp
is mentioned by
dbSNPrs1057524251
dbSNP (old)rs1057524251
ClinGenrs1057524251
ebirs1057524251
HLIrs1057524251
Exacrs1057524251
Gnomadrs1057524251
Varsomers1057524251
Maprs1057524251
PheGenIrs1057524251
Biobankrs1057524251
1000 genomesrs1057524251
hgdprs1057524251
ensemblrs1057524251
gopubmedrs1057524251
geneviewrs1057524251
scholarrs1057524251
googlers1057524251
pharmgkbrs1057524251
gwascentralrs1057524251
openSNPrs1057524251
23andMers1057524251
23andMe allrs1057524251
SNPshotrs1057524251
SNPdbers1057524251
MSV3drs1057524251
GWAS Ctlgrs1057524251
Max Magnitude0
ClinVar
Risk rs1057524251(C;C)
Alt rs1057524251(C;C)
Reference Rs1057524251(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PLOD2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.145804572A>G
CLNSRC
CLNACC RCV000438142.1,