rs863223720
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AAGA;AAGA) | 0 | common in clinvar |
Make rs863223720(-;-) |
Make rs863223720(-;AAGA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 87331426 |
Gene | CCNH, RASA1 |
is a | snp |
is | mentioned by |
dbSNP | rs863223720 |
dbSNP (classic) | rs863223720 |
ClinGen | rs863223720 |
ebi | rs863223720 |
HLI | rs863223720 |
Exac | rs863223720 |
Gnomad | rs863223720 |
Varsome | rs863223720 |
LitVar | rs863223720 |
Map | rs863223720 |
PheGenI | rs863223720 |
Biobank | rs863223720 |
1000 genomes | rs863223720 |
hgdp | rs863223720 |
ensembl | rs863223720 |
geneview | rs863223720 |
scholar | rs863223720 |
rs863223720 | |
pharmgkb | rs863223720 |
gwascentral | rs863223720 |
openSNP | rs863223720 |
23andMe | rs863223720 |
SNPshot | rs863223720 |
SNPdbe | rs863223720 |
MSV3d | rs863223720 |
GWAS Ctlg | rs863223720 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863223720(-;-) |
Alt | rs863223720(-;-) |
Reference | Rs863223720(AAGA;AAGA) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | RASA1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.86627243_86627246delAAGA |
CLNSRC | |
CLNACC | RCV000196235.1, |