rs1127313
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1127313(C;T) |
Make rs1127313(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 154583949 |
Gene | ADAR |
is a | snp |
is | mentioned by |
dbSNP | rs1127313 |
dbSNP (classic) | rs1127313 |
ClinGen | rs1127313 |
ebi | rs1127313 |
HLI | rs1127313 |
Exac | rs1127313 |
Gnomad | rs1127313 |
Varsome | rs1127313 |
LitVar | rs1127313 |
Map | rs1127313 |
PheGenI | rs1127313 |
Biobank | rs1127313 |
1000 genomes | rs1127313 |
hgdp | rs1127313 |
ensembl | rs1127313 |
geneview | rs1127313 |
scholar | rs1127313 |
rs1127313 | |
pharmgkb | rs1127313 |
gwascentral | rs1127313 |
openSNP | rs1127313 |
23andMe | rs1127313 |
SNPshot | rs1127313 |
SNPdbe | rs1127313 |
MSV3d | rs1127313 |
GWAS Ctlg | rs1127313 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 27911851] Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration.
ClinVar | |
---|---|
Risk | rs1127313(T;T) |
Alt | rs1127313(T;T) |
Reference | Rs1127313(C;C) |
Significance | Non-pathogenic |
Disease | Symmetrical dyschromatosis of extremities |
Variation | info |
Gene | ADAR |
CLNDBN | Symmetrical dyschromatosis of extremities |
Reversed | 1 |
HGVS | NC_000001.10:g.154556425G>A |
CLNSRC | |
CLNACC | RCV000301586.1, |