rs587776833
From SNPedia
Orientation | plus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AGA;AGA) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
(TCT;TCT) | 0 | common in clinvar |
(TCTC;TCTC) | 0 | common in clinvar |
Make rs587776833(-;-) |
Make rs587776833(-;AGA) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 180614074 |
Gene | FLT4 |
is a | snp |
is | mentioned by |
dbSNP | rs587776833 |
dbSNP (classic) | rs587776833 |
ClinGen | rs587776833 |
ebi | rs587776833 |
HLI | rs587776833 |
Exac | rs587776833 |
Gnomad | rs587776833 |
Varsome | rs587776833 |
LitVar | rs587776833 |
Map | rs587776833 |
PheGenI | rs587776833 |
Biobank | rs587776833 |
1000 genomes | rs587776833 |
hgdp | rs587776833 |
ensembl | rs587776833 |
geneview | rs587776833 |
scholar | rs587776833 |
rs587776833 | |
pharmgkb | rs587776833 |
gwascentral | rs587776833 |
openSNP | rs587776833 |
23andMe | rs587776833 |
SNPshot | rs587776833 |
SNPdbe | rs587776833 |
MSV3d | rs587776833 |
GWAS Ctlg | rs587776833 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | Rs587776833(AGA;AGA) rs587776833(-;-) |
Alt | Rs587776833(AGA;AGA) rs587776833(-;-) |
Reference | Rs587776833(TCT;TCT) |
Significance | Pathogenic |
Disease | Hereditary lymphedema type I |
Variation | info |
Gene | FLT4 |
CLNDBN | Hereditary lymphedema type I |
Reversed | 1 |
HGVS | NC_000005.9:g.180041074_180041076delAGA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000017656.28, |