rs527236188
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs527236188(C;C) |
Make rs527236188(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 15511 |
Gene | CYTB |
is a | snp |
is | mentioned by |
dbSNP | rs527236188 |
dbSNP (classic) | rs527236188 |
ClinGen | rs527236188 |
ebi | rs527236188 |
HLI | rs527236188 |
Exac | rs527236188 |
Gnomad | rs527236188 |
Varsome | rs527236188 |
LitVar | rs527236188 |
Map | rs527236188 |
PheGenI | rs527236188 |
Biobank | rs527236188 |
1000 genomes | rs527236188 |
hgdp | rs527236188 |
ensembl | rs527236188 |
geneview | rs527236188 |
scholar | rs527236188 |
rs527236188 | |
pharmgkb | rs527236188 |
gwascentral | rs527236188 |
openSNP | rs527236188 |
23andMe | rs527236188 |
SNPshot | rs527236188 |
SNPdbe | rs527236188 |
MSV3d | rs527236188 |
GWAS Ctlg | rs527236188 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs527236188(C;C) |
Alt | rs527236188(C;C) |
Reference | Rs527236188(T;T) |
Significance | Probable-Pathogenic |
Disease | Neoplasm of ovary not provided |
Variation | info |
Gene | CYTB |
CLNDBN | Neoplasm of ovary not provided |
Reversed | 0 |
HGVS | NC_012920.1:m.15511T>C |
CLNSRC | ClinVar |
CLNACC | RCV000133432.1, RCV000223961.1, |