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rs2832616

From SNPedia

Orientationplus
Stabilizedplus
Make rs2832616(C;C)
Make rs2832616(C;T)
Make rs2832616(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position30101474
is asnp
is mentioned by
dbSNPrs2832616
ebirs2832616
HLIrs2832616
Exacrs2832616
Varsomers2832616
Maprs2832616
PheGenIrs2832616
hapmaprs2832616
1000 genomesrs2832616
hgdprs2832616
ensemblrs2832616
gopubmedrs2832616
geneviewrs2832616
scholarrs2832616
googlers2832616
pharmgkbrs2832616
gwascentralrs2832616
openSNPrs2832616
23andMers2832616
23andMe allrs2832616
SNP Nexus

SNPshotrs2832616
SNPdbers2832616
MSV3drs2832616
GWAS Ctlgrs2832616
GMAF0.1951
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23783273OA-icon.png] The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome