rs745305932
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs745305932(A;G) |
Make rs745305932(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 98595424 |
Gene | SLC25A3 |
is a | snp |
is | mentioned by |
dbSNP | rs745305932 |
dbSNP (classic) | rs745305932 |
ClinGen | rs745305932 |
ebi | rs745305932 |
HLI | rs745305932 |
Exac | rs745305932 |
Gnomad | rs745305932 |
Varsome | rs745305932 |
LitVar | rs745305932 |
Map | rs745305932 |
PheGenI | rs745305932 |
Biobank | rs745305932 |
1000 genomes | rs745305932 |
hgdp | rs745305932 |
ensembl | rs745305932 |
geneview | rs745305932 |
scholar | rs745305932 |
rs745305932 | |
pharmgkb | rs745305932 |
gwascentral | rs745305932 |
openSNP | rs745305932 |
23andMe | rs745305932 |
SNPshot | rs745305932 |
SNPdbe | rs745305932 |
MSV3d | rs745305932 |
GWAS Ctlg | rs745305932 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745305932(G;G) |
Alt | rs745305932(G;G) |
Reference | Rs745305932(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC25A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.98989202A>G |
CLNSRC | |
CLNACC | RCV000195488.1, |