rs863223956
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CA;CA) | 0 | common in clinvar |
Make rs863223956(-;-) |
Make rs863223956(-;CA) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 43508053 |
Gene | ETHE1 |
is a | snp |
is | mentioned by |
dbSNP | rs863223956 |
dbSNP (classic) | rs863223956 |
ClinGen | rs863223956 |
ebi | rs863223956 |
HLI | rs863223956 |
Exac | rs863223956 |
Gnomad | rs863223956 |
Varsome | rs863223956 |
LitVar | rs863223956 |
Map | rs863223956 |
PheGenI | rs863223956 |
Biobank | rs863223956 |
1000 genomes | rs863223956 |
hgdp | rs863223956 |
ensembl | rs863223956 |
geneview | rs863223956 |
scholar | rs863223956 |
rs863223956 | |
pharmgkb | rs863223956 |
gwascentral | rs863223956 |
openSNP | rs863223956 |
23andMe | rs863223956 |
SNPshot | rs863223956 |
SNPdbe | rs863223956 |
MSV3d | rs863223956 |
GWAS Ctlg | rs863223956 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863223956(-;-) |
Alt | rs863223956(-;-) |
Reference | Rs863223956(CA;CA) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ETHE1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000019.9:g.44012205_44012206delTG |
CLNSRC | |
CLNACC | RCV000197919.1, |