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rs1871748

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1871748(C;G)
Make rs1871748(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position53213381
GeneCPT2
is asnp
is mentioned by
dbSNPrs1871748
ebirs1871748
HLIrs1871748
Exacrs1871748
Varsomers1871748
Maprs1871748
PheGenIrs1871748
hapmaprs1871748
1000 genomesrs1871748
hgdprs1871748
ensemblrs1871748
gopubmedrs1871748
geneviewrs1871748
scholarrs1871748
googlers1871748
pharmgkbrs1871748
gwascentralrs1871748
openSNPrs1871748
23andMers1871748
23andMe allrs1871748
SNP Nexus

SNPshotrs1871748
SNPdbers1871748
MSV3drs1871748
GWAS Ctlgrs1871748
Max Magnitude0
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs1871748(G;G)
Alt rs1871748(G;G)
Reference rs1871748(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CPT2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.53679053C>G
CLNSRC
CLNACC RCV000185834.1,