rs782349178
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TG;TG) | 0 | common in clinvar |
Make rs782349178(-;-) |
Make rs782349178(-;TG) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 133352135 |
Gene | SURF1 |
is a | snp |
is | mentioned by |
dbSNP | rs782349178 |
dbSNP (classic) | rs782349178 |
ClinGen | rs782349178 |
ebi | rs782349178 |
HLI | rs782349178 |
Exac | rs782349178 |
Gnomad | rs782349178 |
Varsome | rs782349178 |
LitVar | rs782349178 |
Map | rs782349178 |
PheGenI | rs782349178 |
Biobank | rs782349178 |
1000 genomes | rs782349178 |
hgdp | rs782349178 |
ensembl | rs782349178 |
geneview | rs782349178 |
scholar | rs782349178 |
rs782349178 | |
pharmgkb | rs782349178 |
gwascentral | rs782349178 |
openSNP | rs782349178 |
23andMe | rs782349178 |
SNPshot | rs782349178 |
SNPdbe | rs782349178 |
MSV3d | rs782349178 |
GWAS Ctlg | rs782349178 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs782349178(-;-) |
Alt | rs782349178(-;-) |
Reference | Rs782349178(TG;TG) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SURF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.136218990_136218991delTG |
CLNSRC | |
CLNACC | RCV000413343.1, |