rs1057518977
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1057518977(G;T) |
Make rs1057518977(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 67164969 |
Gene | SMAD3 |
is a | snp |
is | mentioned by |
dbSNP | rs1057518977 |
dbSNP (classic) | rs1057518977 |
ClinGen | rs1057518977 |
ebi | rs1057518977 |
HLI | rs1057518977 |
Exac | rs1057518977 |
Gnomad | rs1057518977 |
Varsome | rs1057518977 |
LitVar | rs1057518977 |
Map | rs1057518977 |
PheGenI | rs1057518977 |
Biobank | rs1057518977 |
1000 genomes | rs1057518977 |
hgdp | rs1057518977 |
ensembl | rs1057518977 |
geneview | rs1057518977 |
scholar | rs1057518977 |
rs1057518977 | |
pharmgkb | rs1057518977 |
gwascentral | rs1057518977 |
openSNP | rs1057518977 |
23andMe | rs1057518977 |
SNPshot | rs1057518977 |
SNPdbe | rs1057518977 |
MSV3d | rs1057518977 |
GWAS Ctlg | rs1057518977 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057518977(T;T) |
Alt | rs1057518977(T;T) |
Reference | Rs1057518977(G;G) |
Significance | Probable-Pathogenic |
Disease | Aneurysm |
Variation | info |
Gene | SMAD3 |
CLNDBN | Aneurysm |
Reversed | 0 |
HGVS | NC_000015.9:g.67457307G>T |
CLNSRC | |
CLNACC | RCV000415342.1, |