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rs1114620

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs1114620(A;G)
Make rs1114620(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position9169880
is asnp
is mentioned by
dbSNPrs1114620
dbSNP (classic)rs1114620
ClinGenrs1114620
ebirs1114620
HLIrs1114620
Exacrs1114620
Gnomadrs1114620
Varsomers1114620
LitVarrs1114620
Maprs1114620
PheGenIrs1114620
Biobankrs1114620
1000 genomesrs1114620
hgdprs1114620
ensemblrs1114620
geneviewrs1114620
scholarrs1114620
googlers1114620
pharmgkbrs1114620
gwascentralrs1114620
openSNPrs1114620
23andMers1114620
SNPshotrs1114620
SNPdbers1114620
MSV3drs1114620
GWAS Ctlgrs1114620
GMAF0.1272
Max Magnitude0

This SNP was (previously) easy to confuse with a different SNP, rs11146020, due to the similarity in the number and a current error in the OMIM database, which erroneously cites this SNP, rs1114620, in the first paragraph about Molecular Genetics on this webpage, where the correct citation for the Rice et al. paper [PMID 11326295] should be to rs11146020.

? (A;A) (A;G) (G;G) 28