rs373510719
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs373510719(G;G) |
Make rs373510719(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 48434711 |
Gene | FBN1 |
is a | snp |
is | mentioned by |
dbSNP | rs373510719 |
dbSNP (classic) | rs373510719 |
ClinGen | rs373510719 |
ebi | rs373510719 |
HLI | rs373510719 |
Exac | rs373510719 |
Gnomad | rs373510719 |
Varsome | rs373510719 |
LitVar | rs373510719 |
Map | rs373510719 |
PheGenI | rs373510719 |
Biobank | rs373510719 |
1000 genomes | rs373510719 |
hgdp | rs373510719 |
ensembl | rs373510719 |
geneview | rs373510719 |
scholar | rs373510719 |
rs373510719 | |
pharmgkb | rs373510719 |
gwascentral | rs373510719 |
openSNP | rs373510719 |
23andMe | rs373510719 |
SNPshot | rs373510719 |
SNPdbe | rs373510719 |
MSV3d | rs373510719 |
GWAS Ctlg | rs373510719 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs373510719(G;G) |
Alt | rs373510719(G;G) |
Reference | Rs373510719(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FBN1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.48726908T>G |
CLNSRC | |
CLNACC | RCV000181702.2, |