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rs2048485

From SNPedia

Orientationplus
Stabilizedplus
Make rs2048485(C;C)
Make rs2048485(C;T)
Make rs2048485(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position44510702
GeneLINC01478
is asnp
is mentioned by
dbSNPrs2048485
dbSNP (classic)rs2048485
ClinGenrs2048485
ebirs2048485
HLIrs2048485
Exacrs2048485
Gnomadrs2048485
Varsomers2048485
LitVarrs2048485
Maprs2048485
PheGenIrs2048485
Biobankrs2048485
1000 genomesrs2048485
hgdprs2048485
ensemblrs2048485
geneviewrs2048485
scholarrs2048485
googlers2048485
pharmgkbrs2048485
gwascentralrs2048485
openSNPrs2048485
23andMers2048485
SNPshotrs2048485
SNPdbers2048485
MSV3drs2048485
GWAS Ctlgrs2048485
GMAF0.2006
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22885689OA-icon.png]
Trait Schizophrenia
Title Genome-wide association study of multiplex schizophrenia pedigrees.
Risk Allele
P-val 8E-6
Odds Ratio 1.40 [NR]