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rs2169650

From SNPedia

Orientationminus
Make rs2169650(C;C)
Make rs2169650(C;T)
Make rs2169650(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67596446
is asnp
is mentioned by
dbSNPrs2169650
ebirs2169650
HLIrs2169650
Exacrs2169650
Varsomers2169650
Maprs2169650
PheGenIrs2169650
hapmaprs2169650
1000 genomesrs2169650
hgdprs2169650
ensemblrs2169650
gopubmedrs2169650
geneviewrs2169650
scholarrs2169650
googlers2169650
pharmgkbrs2169650
gwascentralrs2169650
openSNPrs2169650
23andMers2169650
23andMe allrs2169650
SNP Nexus

SNPshotrs2169650
SNPdbers2169650
MSV3drs2169650
GWAS Ctlgrs2169650
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26612412] A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects.