rs1343879
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common on affy axiom data |
Make rs1343879(A;A) |
Make rs1343879(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 75784694 |
Gene | LOC107985664, MAGEE2 |
is a | snp |
is | mentioned by |
dbSNP | rs1343879 |
dbSNP (classic) | rs1343879 |
ClinGen | rs1343879 |
ebi | rs1343879 |
HLI | rs1343879 |
Exac | rs1343879 |
Gnomad | rs1343879 |
Varsome | rs1343879 |
LitVar | rs1343879 |
Map | rs1343879 |
PheGenI | rs1343879 |
Biobank | rs1343879 |
1000 genomes | rs1343879 |
hgdp | rs1343879 |
ensembl | rs1343879 |
geneview | rs1343879 |
scholar | rs1343879 |
rs1343879 | |
pharmgkb | rs1343879 |
gwascentral | rs1343879 |
openSNP | rs1343879 |
23andMe | rs1343879 |
SNPshot | rs1343879 |
SNPdbe | rs1343879 |
MSV3d | rs1343879 |
GWAS Ctlg | rs1343879 |
GMAF | 0.2975 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19200524] A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.