rs767780913
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs767780913(-;GA) |
Make rs767780913(GA;GA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 158114843 |
Gene | SERAC1 |
is a | snp |
is | mentioned by |
dbSNP | rs767780913 |
dbSNP (classic) | rs767780913 |
ClinGen | rs767780913 |
ebi | rs767780913 |
HLI | rs767780913 |
Exac | rs767780913 |
Gnomad | rs767780913 |
Varsome | rs767780913 |
LitVar | rs767780913 |
Map | rs767780913 |
PheGenI | rs767780913 |
Biobank | rs767780913 |
1000 genomes | rs767780913 |
hgdp | rs767780913 |
ensembl | rs767780913 |
geneview | rs767780913 |
scholar | rs767780913 |
rs767780913 | |
pharmgkb | rs767780913 |
gwascentral | rs767780913 |
openSNP | rs767780913 |
23andMe | rs767780913 |
SNPshot | rs767780913 |
SNPdbe | rs767780913 |
MSV3d | rs767780913 |
GWAS Ctlg | rs767780913 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767780913(AG;AG) |
Alt | rs767780913(AG;AG) |
Reference | Rs767780913(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SERAC1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.158535876_158535877dupAG |
CLNSRC | |
CLNACC | RCV000195622.1, |