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rs547662448

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs547662448(A;A)
Make rs547662448(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position2920334
GeneLPIN2
is asnp
is mentioned by
dbSNPrs547662448
ebirs547662448
HLIrs547662448
Exacrs547662448
Varsomers547662448
Maprs547662448
PheGenIrs547662448
hapmaprs547662448
1000 genomesrs547662448
hgdprs547662448
ensemblrs547662448
gopubmedrs547662448
geneviewrs547662448
scholarrs547662448
googlers547662448
pharmgkbrs547662448
gwascentralrs547662448
openSNPrs547662448
23andMers547662448
23andMe allrs547662448
SNP Nexus

SNPshotrs547662448
SNPdbers547662448
MSV3drs547662448
GWAS Ctlgrs547662448
Max Magnitude0
ClinVar
Risk rs547662448(A;A)
Alt rs547662448(A;A)
Reference rs547662448(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LPIN2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.2920332G>A
CLNSRC
CLNACC RCV000222683.1,