rs370898100
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs370898100(A;A) |
Make rs370898100(A;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 13 |
Position | 47988596 |
Gene | SUCLA2 |
is a | snp |
is | mentioned by |
dbSNP | rs370898100 |
dbSNP (classic) | rs370898100 |
ClinGen | rs370898100 |
ebi | rs370898100 |
HLI | rs370898100 |
Exac | rs370898100 |
Gnomad | rs370898100 |
Varsome | rs370898100 |
LitVar | rs370898100 |
Map | rs370898100 |
PheGenI | rs370898100 |
Biobank | rs370898100 |
1000 genomes | rs370898100 |
hgdp | rs370898100 |
ensembl | rs370898100 |
geneview | rs370898100 |
scholar | rs370898100 |
rs370898100 | |
pharmgkb | rs370898100 |
gwascentral | rs370898100 |
openSNP | rs370898100 |
23andMe | rs370898100 |
SNPshot | rs370898100 |
SNPdbe | rs370898100 |
MSV3d | rs370898100 |
GWAS Ctlg | rs370898100 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs370898100(A;A) rs370898100(T;T) |
Alt | rs370898100(A;A) rs370898100(T;T) |
Reference | Rs370898100(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SUCLA2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000013.10:g.48562731C>T |
CLNSRC | |
CLNACC | RCV000186180.1, |