rs200702528
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs200702528(C;C) |
Make rs200702528(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 133352719 |
Gene | SURF1 |
is a | snp |
is | mentioned by |
dbSNP | rs200702528 |
dbSNP (classic) | rs200702528 |
ClinGen | rs200702528 |
ebi | rs200702528 |
HLI | rs200702528 |
Exac | rs200702528 |
Gnomad | rs200702528 |
Varsome | rs200702528 |
LitVar | rs200702528 |
Map | rs200702528 |
PheGenI | rs200702528 |
Biobank | rs200702528 |
1000 genomes | rs200702528 |
hgdp | rs200702528 |
ensembl | rs200702528 |
geneview | rs200702528 |
scholar | rs200702528 |
rs200702528 | |
pharmgkb | rs200702528 |
gwascentral | rs200702528 |
openSNP | rs200702528 |
23andMe | rs200702528 |
SNPshot | rs200702528 |
SNPdbe | rs200702528 |
MSV3d | rs200702528 |
GWAS Ctlg | rs200702528 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200702528(C;C) |
Alt | rs200702528(C;C) |
Reference | Rs200702528(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SURF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.136219574T>C |
CLNSRC | |
CLNACC | RCV000196814.1, |