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

rs12109442

From SNPedia

Orientationplus
Stabilizedplus
Make rs12109442(A;A)
Make rs12109442(A;T)
Make rs12109442(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position95827931
is asnp
is mentioned by
dbSNPrs12109442
dbSNP (old)rs12109442
ClinGenrs12109442
ebirs12109442
HLIrs12109442
Exacrs12109442
Gnomadrs12109442
Varsomers12109442
LitVarrs12109442
Maprs12109442
PheGenIrs12109442
Biobankrs12109442
1000 genomesrs12109442
hgdprs12109442
ensemblrs12109442
gopubmedrs12109442
geneviewrs12109442
scholarrs12109442
googlers12109442
pharmgkbrs12109442
gwascentralrs12109442
openSNPrs12109442
23andMers12109442
23andMe allrs12109442
SNPshotrs12109442
SNPdbers12109442
MSV3drs12109442
GWAS Ctlgrs12109442
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 29399948] A parent-of-origin analysis of paternal genetic variants and increased risk of conotruncal heart defects.