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rs1064797075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position19955969
GeneLPL
is asnp
is mentioned by
dbSNPrs1064797075
dbSNP (old)rs1064797075
ClinGenrs1064797075
ebirs1064797075
HLIrs1064797075
Exacrs1064797075
Gnomadrs1064797075
Varsomers1064797075
Maprs1064797075
PheGenIrs1064797075
Biobankrs1064797075
1000 genomesrs1064797075
hgdprs1064797075
ensemblrs1064797075
gopubmedrs1064797075
geneviewrs1064797075
scholarrs1064797075
googlers1064797075
pharmgkbrs1064797075
gwascentralrs1064797075
openSNPrs1064797075
23andMers1064797075
23andMe allrs1064797075
SNPshotrs1064797075
SNPdbers1064797075
MSV3drs1064797075
GWAS Ctlgrs1064797075
Max Magnitude0
ClinVar
Risk rs1064797075(C;C)
Alt rs1064797075(C;C)
Reference Rs1064797075(T;T)
Significance Probable-Pathogenic
Disease Hyperlipidemia
Variation info
Gene LPL
CLNDBN Hyperlipidemia, familial combined
Reversed 0
HGVS NC_000008.10:g.19813480T>C
CLNSRC
CLNACC RCV000487457.1,