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rs377406897

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377406897(C;T)
Make rs377406897(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position11974738
GenePLOD1
is asnp
is mentioned by
dbSNPrs377406897
dbSNP (classic)rs377406897
ClinGenrs377406897
ebirs377406897
HLIrs377406897
Exacrs377406897
Gnomadrs377406897
Varsomers377406897
LitVarrs377406897
Maprs377406897
PheGenIrs377406897
Biobankrs377406897
1000 genomesrs377406897
hgdprs377406897
ensemblrs377406897
geneviewrs377406897
scholarrs377406897
googlers377406897
pharmgkbrs377406897
gwascentralrs377406897
openSNPrs377406897
23andMers377406897
SNPshotrs377406897
SNPdbers377406897
MSV3drs377406897
GWAS Ctlgrs377406897
Max Magnitude0
ClinVar
Risk rs377406897(T;T)
Alt rs377406897(T;T)
Reference Rs377406897(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PLOD1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.12034795C>T
CLNSRC
CLNACC RCV000479022.1,