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rs876660982

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660982(-;-)
Make rs876660982(-;GTGT)
Make rs876660982(GTGT;GTGT)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position2960705
GeneLPIN2
is asnp
is mentioned by
dbSNPrs876660982
ebirs876660982
HLIrs876660982
Exacrs876660982
Varsomers876660982
Maprs876660982
PheGenIrs876660982
hapmaprs876660982
1000 genomesrs876660982
hgdprs876660982
ensemblrs876660982
gopubmedrs876660982
geneviewrs876660982
scholarrs876660982
googlers876660982
pharmgkbrs876660982
gwascentralrs876660982
openSNPrs876660982
23andMers876660982
23andMe allrs876660982
SNP Nexus

SNPshotrs876660982
SNPdbers876660982
MSV3drs876660982
GWAS Ctlgrs876660982
Max Magnitude0
ClinVar
Risk rs876660982(GTGT;GTGT)
Alt rs876660982(GTGT;GTGT)
Reference rs876660982(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LPIN2
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.2960704_2960707dupACAC
CLNSRC
CLNACC RCV000219594.1,