rs199476110
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs199476110(C;C) |
Make rs199476110(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | MT |
Position | 14319 |
Gene | ND6 |
is a | snp |
is | mentioned by |
dbSNP | rs199476110 |
dbSNP (classic) | rs199476110 |
ClinGen | rs199476110 |
ebi | rs199476110 |
HLI | rs199476110 |
Exac | rs199476110 |
Gnomad | rs199476110 |
Varsome | rs199476110 |
LitVar | rs199476110 |
Map | rs199476110 |
PheGenI | rs199476110 |
Biobank | rs199476110 |
1000 genomes | rs199476110 |
hgdp | rs199476110 |
ensembl | rs199476110 |
geneview | rs199476110 |
scholar | rs199476110 |
rs199476110 | |
pharmgkb | rs199476110 |
gwascentral | rs199476110 |
openSNP | rs199476110 |
23andMe | rs199476110 |
SNPshot | rs199476110 |
SNPdbe | rs199476110 |
MSV3d | rs199476110 |
GWAS Ctlg | rs199476110 |
GMAF | 0.001871 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199476110(C;C) |
Alt | rs199476110(C;C) |
Reference | Rs199476110(T;T) |
Significance | Other |
Disease | Parkinson disease 6 |
Variation | info |
Gene | ND6 |
CLNDBN | Parkinson disease 6, autosomal recessive early-onset |
Reversed | 0 |
HGVS | NC_012920.1:m.14319T>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000010335.3, |