rs527236187
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs527236187(C;C) |
Make rs527236187(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 15470 |
Gene | CYTB |
is a | snp |
is | mentioned by |
dbSNP | rs527236187 |
dbSNP (classic) | rs527236187 |
ClinGen | rs527236187 |
ebi | rs527236187 |
HLI | rs527236187 |
Exac | rs527236187 |
Gnomad | rs527236187 |
Varsome | rs527236187 |
LitVar | rs527236187 |
Map | rs527236187 |
PheGenI | rs527236187 |
Biobank | rs527236187 |
1000 genomes | rs527236187 |
hgdp | rs527236187 |
ensembl | rs527236187 |
geneview | rs527236187 |
scholar | rs527236187 |
rs527236187 | |
pharmgkb | rs527236187 |
gwascentral | rs527236187 |
openSNP | rs527236187 |
23andMe | rs527236187 |
SNPshot | rs527236187 |
SNPdbe | rs527236187 |
MSV3d | rs527236187 |
GWAS Ctlg | rs527236187 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs527236187(C;C) |
Alt | rs527236187(C;C) |
Reference | Rs527236187(T;T) |
Significance | Probable-Pathogenic |
Disease | Familial cancer of breast not provided |
Variation | info |
Gene | CYTB |
CLNDBN | Familial cancer of breast not provided |
Reversed | 0 |
HGVS | NC_012920.1:m.15470T>C |
CLNSRC | ClinVar |
CLNACC | RCV000133431.1, RCV000224601.1, |