rs782623477
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs782623477(A;A) |
Make rs782623477(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 9 |
Position | 133352509 |
Gene | SURF1 |
is a | snp |
is | mentioned by |
dbSNP | rs782623477 |
dbSNP (classic) | rs782623477 |
ClinGen | rs782623477 |
ebi | rs782623477 |
HLI | rs782623477 |
Exac | rs782623477 |
Gnomad | rs782623477 |
Varsome | rs782623477 |
LitVar | rs782623477 |
Map | rs782623477 |
PheGenI | rs782623477 |
Biobank | rs782623477 |
1000 genomes | rs782623477 |
hgdp | rs782623477 |
ensembl | rs782623477 |
geneview | rs782623477 |
scholar | rs782623477 |
rs782623477 | |
pharmgkb | rs782623477 |
gwascentral | rs782623477 |
openSNP | rs782623477 |
23andMe | rs782623477 |
SNPshot | rs782623477 |
SNPdbe | rs782623477 |
MSV3d | rs782623477 |
GWAS Ctlg | rs782623477 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs782623477(A;A) |
Alt | rs782623477(A;A) |
Reference | Rs782623477(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SURF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.136219364G>A |
CLNSRC | |
CLNACC | RCV000321649.1, |