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rs1343879

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs1343879(A;A)
Make rs1343879(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position75784694
GeneMAGEE2
is asnp
is mentioned by
dbSNPrs1343879
ebirs1343879
HLIrs1343879
Exacrs1343879
Varsomers1343879
Maprs1343879
PheGenIrs1343879
hapmaprs1343879
1000 genomesrs1343879
hgdprs1343879
ensemblrs1343879
gopubmedrs1343879
geneviewrs1343879
scholarrs1343879
googlers1343879
pharmgkbrs1343879
gwascentralrs1343879
openSNPrs1343879
23andMers1343879
23andMe allrs1343879
SNP Nexus

SNPshotrs1343879
SNPdbers1343879
MSV3drs1343879
GWAS Ctlgrs1343879
GMAF0.2975
Max Magnitude0
? (A;A) (A;C) (C;C) 28
OMIM300760
DescMELANOMA ANTIGEN, FAMILY E, 2; MAGEE2
Variant
Relatedalso
[PMID 19200524OA-icon.png] A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.


GET Evidence
MAGEE2-E120X
aa_change Glu120Stop
aa_change_short E120X
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0300194
summary