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rs1057524250

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524250(C;C)
Make rs1057524250(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position146071323
GenePLOD2
is asnp
is mentioned by
dbSNPrs1057524250
dbSNP (old)rs1057524250
ClinGenrs1057524250
ebirs1057524250
HLIrs1057524250
Exacrs1057524250
Gnomadrs1057524250
Varsomers1057524250
Maprs1057524250
PheGenIrs1057524250
Biobankrs1057524250
1000 genomesrs1057524250
hgdprs1057524250
ensemblrs1057524250
gopubmedrs1057524250
geneviewrs1057524250
scholarrs1057524250
googlers1057524250
pharmgkbrs1057524250
gwascentralrs1057524250
openSNPrs1057524250
23andMers1057524250
23andMe allrs1057524250
SNPshotrs1057524250
SNPdbers1057524250
MSV3drs1057524250
GWAS Ctlgrs1057524250
Max Magnitude0
ClinVar
Risk rs1057524250(C;C)
Alt rs1057524250(C;C)
Reference Rs1057524250(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PLOD2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.145789110A>G
CLNSRC
CLNACC RCV000427467.1,