rs1172052
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs1172052(C;C) |
Make rs1172052(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 23803152 |
Gene | MIPEP |
is a | snp |
is | mentioned by |
dbSNP | rs1172052 |
dbSNP (classic) | rs1172052 |
ClinGen | rs1172052 |
ebi | rs1172052 |
HLI | rs1172052 |
Exac | rs1172052 |
Gnomad | rs1172052 |
Varsome | rs1172052 |
LitVar | rs1172052 |
Map | rs1172052 |
PheGenI | rs1172052 |
Biobank | rs1172052 |
1000 genomes | rs1172052 |
hgdp | rs1172052 |
ensembl | rs1172052 |
geneview | rs1172052 |
scholar | rs1172052 |
rs1172052 | |
pharmgkb | rs1172052 |
gwascentral | rs1172052 |
openSNP | rs1172052 |
23andMe | rs1172052 |
SNPshot | rs1172052 |
SNPdbe | rs1172052 |
MSV3d | rs1172052 |
GWAS Ctlg | rs1172052 |
Max Magnitude | 0 |
[PMID 20400777] Common variants in cardiac ion channel genes are associated with sudden cardiac death