rs863223955
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs863223955(-;A) |
Make rs863223955(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 43526519 |
Gene | ETHE1 |
is a | snp |
is | mentioned by |
dbSNP | rs863223955 |
dbSNP (classic) | rs863223955 |
ClinGen | rs863223955 |
ebi | rs863223955 |
HLI | rs863223955 |
Exac | rs863223955 |
Gnomad | rs863223955 |
Varsome | rs863223955 |
LitVar | rs863223955 |
Map | rs863223955 |
PheGenI | rs863223955 |
Biobank | rs863223955 |
1000 genomes | rs863223955 |
hgdp | rs863223955 |
ensembl | rs863223955 |
geneview | rs863223955 |
scholar | rs863223955 |
rs863223955 | |
pharmgkb | rs863223955 |
gwascentral | rs863223955 |
openSNP | rs863223955 |
23andMe | rs863223955 |
SNPshot | rs863223955 |
SNPdbe | rs863223955 |
MSV3d | rs863223955 |
GWAS Ctlg | rs863223955 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863223955(A;A) |
Alt | rs863223955(A;A) |
Reference | Rs863223955(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ETHE1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000019.9:g.44030672dupT |
CLNSRC | |
CLNACC | RCV000198962.1, |