rs782024654
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs782024654(A;G) |
Make rs782024654(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 133354713 |
Gene | SURF1, SURF2 |
is a | snp |
is | mentioned by |
dbSNP | rs782024654 |
dbSNP (classic) | rs782024654 |
ClinGen | rs782024654 |
ebi | rs782024654 |
HLI | rs782024654 |
Exac | rs782024654 |
Gnomad | rs782024654 |
Varsome | rs782024654 |
LitVar | rs782024654 |
Map | rs782024654 |
PheGenI | rs782024654 |
Biobank | rs782024654 |
1000 genomes | rs782024654 |
hgdp | rs782024654 |
ensembl | rs782024654 |
geneview | rs782024654 |
scholar | rs782024654 |
rs782024654 | |
pharmgkb | rs782024654 |
gwascentral | rs782024654 |
openSNP | rs782024654 |
23andMe | rs782024654 |
SNPshot | rs782024654 |
SNPdbe | rs782024654 |
MSV3d | rs782024654 |
GWAS Ctlg | rs782024654 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs782024654(G;G) |
Alt | rs782024654(G;G) |
Reference | Rs782024654(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SURF2 SURF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.136221568A>G |
CLNSRC | |
CLNACC | RCV000437222.1, |