rs869025597
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs869025597(G;T) |
Make rs869025597(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 88722285 |
Gene | PIEZO1 |
is a | snp |
is | mentioned by |
dbSNP | rs869025597 |
dbSNP (classic) | rs869025597 |
ClinGen | rs869025597 |
ebi | rs869025597 |
HLI | rs869025597 |
Exac | rs869025597 |
Gnomad | rs869025597 |
Varsome | rs869025597 |
LitVar | rs869025597 |
Map | rs869025597 |
PheGenI | rs869025597 |
Biobank | rs869025597 |
1000 genomes | rs869025597 |
hgdp | rs869025597 |
ensembl | rs869025597 |
geneview | rs869025597 |
scholar | rs869025597 |
rs869025597 | |
pharmgkb | rs869025597 |
gwascentral | rs869025597 |
openSNP | rs869025597 |
23andMe | rs869025597 |
SNPshot | rs869025597 |
SNPdbe | rs869025597 |
MSV3d | rs869025597 |
GWAS Ctlg | rs869025597 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869025597(T;T) |
Alt | rs869025597(T;T) |
Reference | Rs869025597(G;G) |
Significance | Pathogenic |
Disease | Lymphedema |
Variation | info |
Gene | PIEZO1 |
CLNDBN | Lymphedema, hereditary, III |
Reversed | 1 |
HGVS | NC_000016.9:g.88788693C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000208750.2, |