rs782289759
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs782289759(-;GCAG) |
Make rs782289759(GCAG;GCAG) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 133352707 |
Gene | SURF1 |
is a | snp |
is | mentioned by |
dbSNP | rs782289759 |
dbSNP (classic) | rs782289759 |
ClinGen | rs782289759 |
ebi | rs782289759 |
HLI | rs782289759 |
Exac | rs782289759 |
Gnomad | rs782289759 |
Varsome | rs782289759 |
LitVar | rs782289759 |
Map | rs782289759 |
PheGenI | rs782289759 |
Biobank | rs782289759 |
1000 genomes | rs782289759 |
hgdp | rs782289759 |
ensembl | rs782289759 |
geneview | rs782289759 |
scholar | rs782289759 |
rs782289759 | |
pharmgkb | rs782289759 |
gwascentral | rs782289759 |
openSNP | rs782289759 |
23andMe | rs782289759 |
SNPshot | rs782289759 |
SNPdbe | rs782289759 |
MSV3d | rs782289759 |
GWAS Ctlg | rs782289759 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs782289759(GCAG;GCAG) |
Alt | rs782289759(GCAG;GCAG) |
Reference | Rs782289759(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SURF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.136219562_136219563insGCAG |
CLNSRC | |
CLNACC | RCV000478177.1, |