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rs756933588

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756933588(C;T)
Make rs756933588(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position2929065
GeneLPIN2
is asnp
is mentioned by
dbSNPrs756933588
ebirs756933588
HLIrs756933588
Exacrs756933588
Varsomers756933588
Maprs756933588
PheGenIrs756933588
hapmaprs756933588
1000 genomesrs756933588
hgdprs756933588
ensemblrs756933588
gopubmedrs756933588
geneviewrs756933588
scholarrs756933588
googlers756933588
pharmgkbrs756933588
gwascentralrs756933588
openSNPrs756933588
23andMers756933588
23andMe allrs756933588
SNP Nexus

SNPshotrs756933588
SNPdbers756933588
MSV3drs756933588
GWAS Ctlgrs756933588
Max Magnitude0
ClinVar
Risk rs756933588(T;T)
Alt rs756933588(T;T)
Reference rs756933588(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LPIN2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.2929063C>T
CLNSRC
CLNACC RCV000217293.1,