rs193302982
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs193302982(C;C) |
Make rs193302982(C;T) |
Make rs193302982(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 14783 |
Gene | CYTB |
is a | snp |
is | mentioned by |
dbSNP | rs193302982 |
dbSNP (classic) | rs193302982 |
ClinGen | rs193302982 |
ebi | rs193302982 |
HLI | rs193302982 |
Exac | rs193302982 |
Gnomad | rs193302982 |
Varsome | rs193302982 |
LitVar | rs193302982 |
Map | rs193302982 |
PheGenI | rs193302982 |
Biobank | rs193302982 |
1000 genomes | rs193302982 |
hgdp | rs193302982 |
ensembl | rs193302982 |
geneview | rs193302982 |
scholar | rs193302982 |
rs193302982 | |
pharmgkb | rs193302982 |
gwascentral | rs193302982 |
openSNP | rs193302982 |
23andMe | rs193302982 |
SNPshot | rs193302982 |
SNPdbe | rs193302982 |
MSV3d | rs193302982 |
GWAS Ctlg | rs193302982 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs193302982(C;C) rs193302982(G;G) rs193302982(T;T) |
Alt | rs193302982(C;C) rs193302982(G;G) rs193302982(T;T) |
Reference | Rs193302982(A;A) |
Significance | Probable-Pathogenic |
Disease | Familial cancer of breast |
Variation | info |
Gene | CYTB |
CLNDBN | Familial cancer of breast |
Reversed | 1 |
HGVS | NC_012920.1:m.14783T>C |
CLNSRC | |
CLNACC | RCV000128803.1, |