rs765028734
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs765028734(-;G) |
Make rs765028734(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 32081646 |
Gene | TNXB |
is a | snp |
is | mentioned by |
dbSNP | rs765028734 |
dbSNP (classic) | rs765028734 |
ClinGen | rs765028734 |
ebi | rs765028734 |
HLI | rs765028734 |
Exac | rs765028734 |
Gnomad | rs765028734 |
Varsome | rs765028734 |
LitVar | rs765028734 |
Map | rs765028734 |
PheGenI | rs765028734 |
Biobank | rs765028734 |
1000 genomes | rs765028734 |
hgdp | rs765028734 |
ensembl | rs765028734 |
geneview | rs765028734 |
scholar | rs765028734 |
rs765028734 | |
pharmgkb | rs765028734 |
gwascentral | rs765028734 |
openSNP | rs765028734 |
23andMe | rs765028734 |
SNPshot | rs765028734 |
SNPdbe | rs765028734 |
MSV3d | rs765028734 |
GWAS Ctlg | rs765028734 |
Max Magnitude | 0 |
aka c.3762_3763dupGG, and also delG & dupG
ClinVar | |
---|---|
Risk | rs765028734(G;G) rs765028734(GG;GG) |
Alt | rs765028734(G;G) rs765028734(GG;GG) |
Reference | Rs765028734(-;-) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TNXB |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.32049423_32049424insGG |
CLNSRC | |
CLNACC | RCV000487708.1, |