rs772339721
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs772339721(A;T) |
Make rs772339721(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 99137964 |
Gene | TGFBR1 |
is a | snp |
is | mentioned by |
dbSNP | rs772339721 |
dbSNP (classic) | rs772339721 |
ClinGen | rs772339721 |
ebi | rs772339721 |
HLI | rs772339721 |
Exac | rs772339721 |
Gnomad | rs772339721 |
Varsome | rs772339721 |
LitVar | rs772339721 |
Map | rs772339721 |
PheGenI | rs772339721 |
Biobank | rs772339721 |
1000 genomes | rs772339721 |
hgdp | rs772339721 |
ensembl | rs772339721 |
geneview | rs772339721 |
scholar | rs772339721 |
rs772339721 | |
pharmgkb | rs772339721 |
gwascentral | rs772339721 |
openSNP | rs772339721 |
23andMe | rs772339721 |
SNPshot | rs772339721 |
SNPdbe | rs772339721 |
MSV3d | rs772339721 |
GWAS Ctlg | rs772339721 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772339721(G;G) rs772339721(T;T) |
Alt | rs772339721(G;G) rs772339721(T;T) |
Reference | Rs772339721(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TGFBR1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.101900246A>T |
CLNSRC | |
CLNACC | RCV000483348.1, |