rs776969714
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(D;D) | 0 | common genotype |
Make rs776969714(-;C) |
Make rs776969714(C;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 4 |
Position | 25145129 |
Gene | SEPSECS |
is a | snp |
is | mentioned by |
dbSNP | rs776969714 |
dbSNP (classic) | rs776969714 |
ClinGen | rs776969714 |
ebi | rs776969714 |
HLI | rs776969714 |
Exac | rs776969714 |
Gnomad | rs776969714 |
Varsome | rs776969714 |
LitVar | rs776969714 |
Map | rs776969714 |
PheGenI | rs776969714 |
Biobank | rs776969714 |
1000 genomes | rs776969714 |
hgdp | rs776969714 |
ensembl | rs776969714 |
geneview | rs776969714 |
scholar | rs776969714 |
rs776969714 | |
pharmgkb | rs776969714 |
gwascentral | rs776969714 |
openSNP | rs776969714 |
23andMe | rs776969714 |
SNPshot | rs776969714 |
SNPdbe | rs776969714 |
MSV3d | rs776969714 |
GWAS Ctlg | rs776969714 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776969714(C;C) |
Alt | rs776969714(C;C) |
Reference | Rs776969714(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SEPSECS |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.25146752dupC |
CLNSRC | |
CLNACC | RCV000396553.1, |