Have questions? Visit https://www.reddit.com/r/SNPedia

rs1007190

From SNPedia

Orientationplus
Stabilizedplus
Make rs1007190(C;C)
Make rs1007190(C;T)
Make rs1007190(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position44960841
GeneC1QL1
is asnp
is mentioned by
dbSNPrs1007190
ebirs1007190
HLIrs1007190
Exacrs1007190
Varsomers1007190
Maprs1007190
PheGenIrs1007190
hapmaprs1007190
1000 genomesrs1007190
hgdprs1007190
ensemblrs1007190
gopubmedrs1007190
geneviewrs1007190
scholarrs1007190
googlers1007190
pharmgkbrs1007190
gwascentralrs1007190
openSNPrs1007190
23andMers1007190
23andMe allrs1007190
SNP Nexus

SNPshotrs1007190
SNPdbers1007190
MSV3drs1007190
GWAS Ctlgrs1007190
GMAF0.1492
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23725790]
Trait DNA methylation (variation)
Title GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
Risk Allele T
P-val 2E-6
Odds Ratio NR NR