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rs144261491

From SNPedia

Orientationplus
Stabilizedplus
Make rs144261491(C;C)
Make rs144261491(C;T)
Make rs144261491(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position88838104
GeneMEF2C
is asnp
is mentioned by
dbSNPrs144261491
dbSNP (old)rs144261491
ClinGenrs144261491
ebirs144261491
HLIrs144261491
Exacrs144261491
Gnomadrs144261491
Varsomers144261491
Maprs144261491
PheGenIrs144261491
Biobankrs144261491
1000 genomesrs144261491
hgdprs144261491
ensemblrs144261491
gopubmedrs144261491
geneviewrs144261491
scholarrs144261491
googlers144261491
pharmgkbrs144261491
gwascentralrs144261491
openSNPrs144261491
23andMers144261491
23andMe allrs144261491
SNP Nexus

SNPshotrs144261491
SNPdbers144261491
MSV3drs144261491
GWAS Ctlgrs144261491
Max Magnitude
Said to be an "Amerindian-specific variant" in [PMID 26805783OA-icon.png]; specifically, the allele frequency for the minor (T) allele is around 4% in many South American populations but is undetected in Asian, European and African populations.