rs863223922
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs863223922(A;A) |
Make rs863223922(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 100989706 |
Gene | C10orf2, TWNK |
is a | snp |
is | mentioned by |
dbSNP | rs863223922 |
dbSNP (classic) | rs863223922 |
ClinGen | rs863223922 |
ebi | rs863223922 |
HLI | rs863223922 |
Exac | rs863223922 |
Gnomad | rs863223922 |
Varsome | rs863223922 |
LitVar | rs863223922 |
Map | rs863223922 |
PheGenI | rs863223922 |
Biobank | rs863223922 |
1000 genomes | rs863223922 |
hgdp | rs863223922 |
ensembl | rs863223922 |
geneview | rs863223922 |
scholar | rs863223922 |
rs863223922 | |
pharmgkb | rs863223922 |
gwascentral | rs863223922 |
openSNP | rs863223922 |
23andMe | rs863223922 |
SNPshot | rs863223922 |
SNPdbe | rs863223922 |
MSV3d | rs863223922 |
GWAS Ctlg | rs863223922 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863223922(A;A) |
Alt | rs863223922(A;A) |
Reference | Rs863223922(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | C10orf2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.102749463G>A |
CLNSRC | |
CLNACC | RCV000197887.1, |