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rs374644

From SNPedia

Merged intors360064
Orientationplus
Make rs374644(G;G)
Make rs374644(G;T)
Make rs374644(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome1
Position225918985
is asnp
is mentioned by
dbSNPrs374644
dbSNP (classic)rs374644
ClinGenrs374644
ebirs374644
HLIrs374644
Exacrs374644
Gnomadrs374644
Varsomers374644
LitVarrs374644
Maprs374644
PheGenIrs374644
Biobankrs374644
1000 genomesrs374644
hgdprs374644
ensemblrs374644
geneviewrs374644
scholarrs374644
googlers374644
pharmgkbrs374644
gwascentralrs374644
openSNPrs374644
23andMers374644
SNPshotrs374644
SNPdbers374644
MSV3drs374644
GWAS Ctlgrs374644
StatusMerged into rs360064
Max Magnitude0

[PMID 30084801] Association of a MiR-499 SNP and risk of congenital heart disease in a Chinese population.