rs376710410
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs376710410(A;C) |
Make rs376710410(C;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 3 |
Position | 33065551 |
Gene | GLB1 |
is a | snp |
is | mentioned by |
dbSNP | rs376710410 |
dbSNP (classic) | rs376710410 |
ClinGen | rs376710410 |
ebi | rs376710410 |
HLI | rs376710410 |
Exac | rs376710410 |
Gnomad | rs376710410 |
Varsome | rs376710410 |
LitVar | rs376710410 |
Map | rs376710410 |
PheGenI | rs376710410 |
Biobank | rs376710410 |
1000 genomes | rs376710410 |
hgdp | rs376710410 |
ensembl | rs376710410 |
geneview | rs376710410 |
scholar | rs376710410 |
rs376710410 | |
pharmgkb | rs376710410 |
gwascentral | rs376710410 |
openSNP | rs376710410 |
23andMe | rs376710410 |
SNPshot | rs376710410 |
SNPdbe | rs376710410 |
MSV3d | rs376710410 |
GWAS Ctlg | rs376710410 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs376710410(C;C) |
Alt | rs376710410(C;C) |
Reference | Rs376710410(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TMPPE GLB1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.33107043A>C |
CLNSRC | |
CLNACC | RCV000256106.1, |