rs141295770
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs141295770(A;A) |
Make rs141295770(A;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 13 |
Position | 47949491 |
Gene | SUCLA2 |
is a | snp |
is | mentioned by |
dbSNP | rs141295770 |
dbSNP (classic) | rs141295770 |
ClinGen | rs141295770 |
ebi | rs141295770 |
HLI | rs141295770 |
Exac | rs141295770 |
Gnomad | rs141295770 |
Varsome | rs141295770 |
LitVar | rs141295770 |
Map | rs141295770 |
PheGenI | rs141295770 |
Biobank | rs141295770 |
1000 genomes | rs141295770 |
hgdp | rs141295770 |
ensembl | rs141295770 |
geneview | rs141295770 |
scholar | rs141295770 |
rs141295770 | |
pharmgkb | rs141295770 |
gwascentral | rs141295770 |
openSNP | rs141295770 |
23andMe | rs141295770 |
SNPshot | rs141295770 |
SNPdbe | rs141295770 |
MSV3d | rs141295770 |
GWAS Ctlg | rs141295770 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141295770(A;A) |
Alt | rs141295770(A;A) |
Reference | Rs141295770(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SUCLA2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000013.10:g.48523626C>A |
CLNSRC | |
CLNACC | RCV000186187.1, |