rs759805984
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs759805984(A;A) |
Make rs759805984(A;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 99149213 |
Gene | TGFBR1 |
is a | snp |
is | mentioned by |
dbSNP | rs759805984 |
dbSNP (classic) | rs759805984 |
ClinGen | rs759805984 |
ebi | rs759805984 |
HLI | rs759805984 |
Exac | rs759805984 |
Gnomad | rs759805984 |
Varsome | rs759805984 |
LitVar | rs759805984 |
Map | rs759805984 |
PheGenI | rs759805984 |
Biobank | rs759805984 |
1000 genomes | rs759805984 |
hgdp | rs759805984 |
ensembl | rs759805984 |
geneview | rs759805984 |
scholar | rs759805984 |
rs759805984 | |
pharmgkb | rs759805984 |
gwascentral | rs759805984 |
openSNP | rs759805984 |
23andMe | rs759805984 |
SNPshot | rs759805984 |
SNPdbe | rs759805984 |
MSV3d | rs759805984 |
GWAS Ctlg | rs759805984 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759805984(A;A) rs759805984(C;C) |
Alt | rs759805984(A;A) rs759805984(C;C) |
Reference | Rs759805984(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TGFBR1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.101911495T>C |
CLNSRC | |
CLNACC | RCV000198521.1, |