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rs1890645

From SNPedia

Orientationplus
Stabilizedplus
Make rs1890645(C;C)
Make rs1890645(C;T)
Make rs1890645(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position195562293
is asnp
is mentioned by
dbSNPrs1890645
ebirs1890645
HLIrs1890645
Exacrs1890645
Varsomers1890645
Maprs1890645
PheGenIrs1890645
hapmaprs1890645
1000 genomesrs1890645
hgdprs1890645
ensemblrs1890645
gopubmedrs1890645
geneviewrs1890645
scholarrs1890645
googlers1890645
pharmgkbrs1890645
gwascentralrs1890645
openSNPrs1890645
23andMers1890645
23andMe allrs1890645
SNP Nexus

SNPshotrs1890645
SNPdbers1890645
MSV3drs1890645
GWAS Ctlgrs1890645
GMAF0.3356
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20662065OA-icon.png]
Trait Neonatal lupus
Title Genome-wide association study of cardiac manifestations of neonatal lupus identifies candidate loci at 6p21 and 21q22
Risk Allele
P-val 0.000004
Odds Ratio 2.98 [1.88-4.73]