rs527236165
From SNPedia
Merged into | rs386419981 |
Orientation | minus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs527236165(C;G) |
Make rs527236165(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 14891 |
Gene | MT-CYB |
is a | snp |
is | mentioned by |
dbSNP | rs527236165 |
dbSNP (classic) | rs527236165 |
ClinGen | rs527236165 |
ebi | rs527236165 |
HLI | rs527236165 |
Exac | rs527236165 |
Gnomad | rs527236165 |
Varsome | rs527236165 |
LitVar | rs527236165 |
Map | rs527236165 |
PheGenI | rs527236165 |
Biobank | rs527236165 |
1000 genomes | rs527236165 |
hgdp | rs527236165 |
ensembl | rs527236165 |
geneview | rs527236165 |
scholar | rs527236165 |
rs527236165 | |
pharmgkb | rs527236165 |
gwascentral | rs527236165 |
openSNP | rs527236165 |
23andMe | rs527236165 |
SNPshot | rs527236165 |
SNPdbe | rs527236165 |
MSV3d | rs527236165 |
GWAS Ctlg | rs527236165 |
Status | Merged into rs386419981 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs527236165(G;G) |
Alt | rs527236165(G;G) |
Reference | Rs527236165(C;C) |
Significance | Probable-Pathogenic |
Disease | Familial cancer of breast |
Variation | info |
Gene | CYTB |
CLNDBN | Familial cancer of breast |
Reversed | 0 |
HGVS | NC_012920.1:m.14891C>G |
CLNSRC | ClinVar |
CLNACC | RCV000133407.1, |