rs966681982
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 6703140 |
Gene | SLC13A5 |
is a | snp |
is | mentioned by |
dbSNP | rs966681982 |
dbSNP (classic) | rs966681982 |
ClinGen | rs966681982 |
ebi | rs966681982 |
HLI | rs966681982 |
Exac | rs966681982 |
Gnomad | rs966681982 |
Varsome | rs966681982 |
LitVar | rs966681982 |
Map | rs966681982 |
PheGenI | rs966681982 |
Biobank | rs966681982 |
1000 genomes | rs966681982 |
hgdp | rs966681982 |
ensembl | rs966681982 |
geneview | rs966681982 |
scholar | rs966681982 |
rs966681982 | |
pharmgkb | rs966681982 |
gwascentral | rs966681982 |
openSNP | rs966681982 |
23andMe | rs966681982 |
SNPshot | rs966681982 |
SNPdbe | rs966681982 |
MSV3d | rs966681982 |
GWAS Ctlg | rs966681982 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs966681982(C;C) |
Alt | rs966681982(C;C) |
Reference | Rs966681982(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.6606459T>C |
CLNSRC | |
CLNACC | RCV000485335.1, |