rs781934508
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs781934508(C;T) |
Make rs781934508(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 133352441 |
Gene | SURF1 |
is a | snp |
is | mentioned by |
dbSNP | rs781934508 |
dbSNP (classic) | rs781934508 |
ClinGen | rs781934508 |
ebi | rs781934508 |
HLI | rs781934508 |
Exac | rs781934508 |
Gnomad | rs781934508 |
Varsome | rs781934508 |
LitVar | rs781934508 |
Map | rs781934508 |
PheGenI | rs781934508 |
Biobank | rs781934508 |
1000 genomes | rs781934508 |
hgdp | rs781934508 |
ensembl | rs781934508 |
geneview | rs781934508 |
scholar | rs781934508 |
rs781934508 | |
pharmgkb | rs781934508 |
gwascentral | rs781934508 |
openSNP | rs781934508 |
23andMe | rs781934508 |
SNPshot | rs781934508 |
SNPdbe | rs781934508 |
MSV3d | rs781934508 |
GWAS Ctlg | rs781934508 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs781934508(T;T) |
Alt | rs781934508(T;T) |
Reference | Rs781934508(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SURF1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.136219296C>T |
CLNSRC | |
CLNACC | RCV000413105.1, |