rs886041237
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Chromosome | 11 |
Position | 112087857 |
Gene | SDHD, TIMM8B |
is a | snp |
is | mentioned by |
dbSNP | rs886041237 |
dbSNP (classic) | rs886041237 |
ClinGen | rs886041237 |
ebi | rs886041237 |
HLI | rs886041237 |
Exac | rs886041237 |
Gnomad | rs886041237 |
Varsome | rs886041237 |
LitVar | rs886041237 |
Map | rs886041237 |
PheGenI | rs886041237 |
Biobank | rs886041237 |
1000 genomes | rs886041237 |
hgdp | rs886041237 |
ensembl | rs886041237 |
geneview | rs886041237 |
scholar | rs886041237 |
rs886041237 | |
pharmgkb | rs886041237 |
gwascentral | rs886041237 |
openSNP | rs886041237 |
23andMe | rs886041237 |
SNPshot | rs886041237 |
SNPdbe | rs886041237 |
MSV3d | rs886041237 |
GWAS Ctlg | rs886041237 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041237(C;C) |
Alt | rs886041237(C;C) |
Reference | Rs886041237(-;-) |
Significance | Pathogenic |
Disease | not provided Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | TIMM8B SDHD |
CLNDBN | not provided Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.111958581dupC |
CLNSRC | |
CLNACC | RCV000349345.1, RCV000492278.1, |