rs199795644
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs199795644(A;A) |
Make rs199795644(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 14831 |
Gene | CYTB |
is a | snp |
is | mentioned by |
dbSNP | rs199795644 |
dbSNP (classic) | rs199795644 |
ClinGen | rs199795644 |
ebi | rs199795644 |
HLI | rs199795644 |
Exac | rs199795644 |
Gnomad | rs199795644 |
Varsome | rs199795644 |
LitVar | rs199795644 |
Map | rs199795644 |
PheGenI | rs199795644 |
Biobank | rs199795644 |
1000 genomes | rs199795644 |
hgdp | rs199795644 |
ensembl | rs199795644 |
geneview | rs199795644 |
scholar | rs199795644 |
rs199795644 | |
pharmgkb | rs199795644 |
gwascentral | rs199795644 |
openSNP | rs199795644 |
23andMe | rs199795644 |
SNPshot | rs199795644 |
SNPdbe | rs199795644 |
MSV3d | rs199795644 |
GWAS Ctlg | rs199795644 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199795644(A;A) |
Alt | rs199795644(A;A) |
Reference | Rs199795644(G;G) |
Significance | Pathogenic |
Disease | Leber's optic atrophy |
Variation | info |
Gene | CYTB |
CLNDBN | Leber's optic atrophy |
Reversed | 0 |
HGVS | NC_012920.1:m.14831G>A |
CLNSRC | ClinVar GeneReviews |
CLNACC | RCV000055706.1, |