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rs1943950

From SNPedia

Orientationminus
Stabilizedminus
Make rs1943950(C;C)
Make rs1943950(C;T)
Make rs1943950(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position30107534
is asnp
is mentioned by
dbSNPrs1943950
ebirs1943950
HLIrs1943950
Exacrs1943950
Varsomers1943950
Maprs1943950
PheGenIrs1943950
hapmaprs1943950
1000 genomesrs1943950
hgdprs1943950
ensemblrs1943950
gopubmedrs1943950
geneviewrs1943950
scholarrs1943950
googlers1943950
pharmgkbrs1943950
gwascentralrs1943950
openSNPrs1943950
23andMers1943950
23andMe allrs1943950
SNP Nexus

SNPshotrs1943950
SNPdbers1943950
MSV3drs1943950
GWAS Ctlgrs1943950
GMAF0.1919
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