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rs117672662

From SNPedia

Orientationplus
Stabilizedplus
Make rs117672662(C;C)
Make rs117672662(C;T)
Make rs117672662(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position68958750
GeneACTN1
is asnp
is mentioned by
dbSNPrs117672662
dbSNP (old)rs117672662
ClinGenrs117672662
ebirs117672662
HLIrs117672662
Exacrs117672662
Gnomadrs117672662
Varsomers117672662
Maprs117672662
PheGenIrs117672662
Biobankrs117672662
1000 genomesrs117672662
hgdprs117672662
ensemblrs117672662
gopubmedrs117672662
geneviewrs117672662
scholarrs117672662
googlers117672662
pharmgkbrs117672662
gwascentralrs117672662
openSNPrs117672662
23andMers117672662
23andMe allrs117672662
SNP Nexus

SNPshotrs117672662
SNPdbers117672662
MSV3drs117672662
GWAS Ctlgrs117672662
Max Magnitude
Said to be an "Amerindian-specific variant" in [PMID 26805783OA-icon.png]; specifically, the allele frequency for the minor (C) allele is around 7% in many South American populations but is either undetected or under 1% in Asian, European and African populations.