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rs2853493

From SNPedia

A11467G, defines MT-haplogroup U
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0.1 A11467G-, not MT-Haplogroup U or K.
(G;G) 1 A11467G+, MT-Haplogroup U or K
Make rs2853493(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position11467
GeneND4
is asnp
is mentioned by
dbSNPrs2853493
dbSNP (classic)rs2853493
ClinGenrs2853493
ebirs2853493
HLIrs2853493
Exacrs2853493
Gnomadrs2853493
Varsomers2853493
LitVarrs2853493
Maprs2853493
PheGenIrs2853493
Biobankrs2853493
1000 genomesrs2853493
hgdprs2853493
ensemblrs2853493
geneviewrs2853493
scholarrs2853493
googlers2853493
pharmgkbrs2853493
gwascentralrs2853493
openSNPrs2853493
23andMers2853493
SNPshotrs2853493
SNPdbers2853493
MSV3drs2853493
GWAS Ctlgrs2853493
GMAF0.1001
Max Magnitude1
? (A;A) (A;G) (G;G) 28


More commonly known as A11467G, or 11467. One of 3 Mitochondrial mutations that together define Mitochondrial Haplogroup U, and its descendants. This is a synonymous change that still codes for the exact same amino acid, so it probably has no biological effect.