rs28358572
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common on affy axiom data |
Make rs28358572(C;C) |
Make rs28358572(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 1243 |
is a | snp |
is | mentioned by |
dbSNP | rs28358572 |
dbSNP (classic) | rs28358572 |
ClinGen | rs28358572 |
ebi | rs28358572 |
HLI | rs28358572 |
Exac | rs28358572 |
Gnomad | rs28358572 |
Varsome | rs28358572 |
LitVar | rs28358572 |
Map | rs28358572 |
PheGenI | rs28358572 |
Biobank | rs28358572 |
1000 genomes | rs28358572 |
hgdp | rs28358572 |
ensembl | rs28358572 |
geneview | rs28358572 |
scholar | rs28358572 |
rs28358572 | |
pharmgkb | rs28358572 |
gwascentral | rs28358572 |
openSNP | rs28358572 |
23andMe | rs28358572 |
SNPshot | rs28358572 |
SNPdbe | rs28358572 |
MSV3d | rs28358572 |
GWAS Ctlg | rs28358572 |
GMAF | 0.01123 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 11245424] Detection of mitochondrial DNA mutations in pancreatic cancer offers a "mass"-ive advantage over detection of nuclear DNA mutations.
ClinVar | |
---|---|
Risk | rs28358572(C;C) |
Alt | rs28358572(C;C) |
Reference | Rs28358572(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_012920.1:m.1243T>C |
CLNSRC | |
CLNACC | RCV000035037.2, |