rs139301835
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs139301835(C;C) |
Make rs139301835(C;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 158158343 |
Gene | SERAC1 |
is a | snp |
is | mentioned by |
dbSNP | rs139301835 |
dbSNP (classic) | rs139301835 |
ClinGen | rs139301835 |
ebi | rs139301835 |
HLI | rs139301835 |
Exac | rs139301835 |
Gnomad | rs139301835 |
Varsome | rs139301835 |
LitVar | rs139301835 |
Map | rs139301835 |
PheGenI | rs139301835 |
Biobank | rs139301835 |
1000 genomes | rs139301835 |
hgdp | rs139301835 |
ensembl | rs139301835 |
geneview | rs139301835 |
scholar | rs139301835 |
rs139301835 | |
pharmgkb | rs139301835 |
gwascentral | rs139301835 |
openSNP | rs139301835 |
23andMe | rs139301835 |
SNPshot | rs139301835 |
SNPdbe | rs139301835 |
MSV3d | rs139301835 |
GWAS Ctlg | rs139301835 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139301835(A;A) rs139301835(C;C) |
Alt | rs139301835(A;A) rs139301835(C;C) |
Reference | Rs139301835(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SERAC1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.158579375G>C |
CLNSRC | |
CLNACC | RCV000200793.2, |