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rs17491951

From SNPedia

Orientationminus
Stabilizedminus
Make rs17491951(C;C)
Make rs17491951(C;T)
Make rs17491951(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position2922241
GeneLINC01250
is asnp
is mentioned by
dbSNPrs17491951
dbSNP (classic)rs17491951
ClinGenrs17491951
ebirs17491951
HLIrs17491951
Exacrs17491951
Gnomadrs17491951
Varsomers17491951
LitVarrs17491951
Maprs17491951
PheGenIrs17491951
Biobankrs17491951
1000 genomesrs17491951
hgdprs17491951
ensemblrs17491951
geneviewrs17491951
scholarrs17491951
googlers17491951
pharmgkbrs17491951
gwascentralrs17491951
openSNPrs17491951
23andMers17491951
SNPshotrs17491951
SNPdbers17491951
MSV3drs17491951
GWAS Ctlgrs17491951
GMAF0.2006
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23218918]
Trait White matter integrity (interaction)
Title White matter integrity as an intermediate phenotype: Exploratory genome-wide association analysis in individuals at high risk of bipolar disorder.
Risk Allele
P-val 7E-6
Odds Ratio NR NR