rs1057518299
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs1057518299(-;C) |
Make rs1057518299(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 6693091 |
Gene | SLC13A5 |
is a | snp |
is | mentioned by |
dbSNP | rs1057518299 |
dbSNP (classic) | rs1057518299 |
ClinGen | rs1057518299 |
ebi | rs1057518299 |
HLI | rs1057518299 |
Exac | rs1057518299 |
Gnomad | rs1057518299 |
Varsome | rs1057518299 |
LitVar | rs1057518299 |
Map | rs1057518299 |
PheGenI | rs1057518299 |
Biobank | rs1057518299 |
1000 genomes | rs1057518299 |
hgdp | rs1057518299 |
ensembl | rs1057518299 |
geneview | rs1057518299 |
scholar | rs1057518299 |
rs1057518299 | |
pharmgkb | rs1057518299 |
gwascentral | rs1057518299 |
openSNP | rs1057518299 |
23andMe | rs1057518299 |
SNPshot | rs1057518299 |
SNPdbe | rs1057518299 |
MSV3d | rs1057518299 |
GWAS Ctlg | rs1057518299 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518299(C;C) |
Alt | rs1057518299(C;C) |
Reference | Rs1057518299(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC13A5 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000017.10:g.6596411dupG |
CLNSRC | |
CLNACC | RCV000414557.1, |