rs749890642
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs749890642(A;A) |
Make rs749890642(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 32089277 |
Gene | TNXB |
is a | snp |
is | mentioned by |
dbSNP | rs749890642 |
dbSNP (classic) | rs749890642 |
ClinGen | rs749890642 |
ebi | rs749890642 |
HLI | rs749890642 |
Exac | rs749890642 |
Gnomad | rs749890642 |
Varsome | rs749890642 |
LitVar | rs749890642 |
Map | rs749890642 |
PheGenI | rs749890642 |
Biobank | rs749890642 |
1000 genomes | rs749890642 |
hgdp | rs749890642 |
ensembl | rs749890642 |
geneview | rs749890642 |
scholar | rs749890642 |
rs749890642 | |
pharmgkb | rs749890642 |
gwascentral | rs749890642 |
openSNP | rs749890642 |
23andMe | rs749890642 |
SNPshot | rs749890642 |
SNPdbe | rs749890642 |
MSV3d | rs749890642 |
GWAS Ctlg | rs749890642 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs749890642(A;A) |
Alt | rs749890642(A;A) |
Reference | Rs749890642(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TNXB |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.32057054G>A |
CLNSRC | |
CLNACC | RCV000413590.1, |