rs757504141
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs757504141(C;C) |
Make rs757504141(C;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 4 |
Position | 25156853 |
Gene | SEPSECS |
is a | snp |
is | mentioned by |
dbSNP | rs757504141 |
dbSNP (classic) | rs757504141 |
ClinGen | rs757504141 |
ebi | rs757504141 |
HLI | rs757504141 |
Exac | rs757504141 |
Gnomad | rs757504141 |
Varsome | rs757504141 |
LitVar | rs757504141 |
Map | rs757504141 |
PheGenI | rs757504141 |
Biobank | rs757504141 |
1000 genomes | rs757504141 |
hgdp | rs757504141 |
ensembl | rs757504141 |
geneview | rs757504141 |
scholar | rs757504141 |
rs757504141 | |
pharmgkb | rs757504141 |
gwascentral | rs757504141 |
openSNP | rs757504141 |
23andMe | rs757504141 |
SNPshot | rs757504141 |
SNPdbe | rs757504141 |
MSV3d | rs757504141 |
GWAS Ctlg | rs757504141 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757504141(C;C) |
Alt | rs757504141(C;C) |
Reference | Rs757504141(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SEPSECS |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.25158475T>C |
CLNSRC | |
CLNACC | RCV000428576.1, |