rs587777658
From SNPedia
Orientation | plus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(AG;AG) | 0 | common in clinvar |
(T;T) | 0 | common in clinvar |
Make rs587777658(-;-) |
Make rs587777658(-;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 22 |
Position | 20425445 |
Gene | SCARF2 |
is a | snp |
is | mentioned by |
dbSNP | rs587777658 |
dbSNP (classic) | rs587777658 |
ClinGen | rs587777658 |
ebi | rs587777658 |
HLI | rs587777658 |
Exac | rs587777658 |
Gnomad | rs587777658 |
Varsome | rs587777658 |
LitVar | rs587777658 |
Map | rs587777658 |
PheGenI | rs587777658 |
Biobank | rs587777658 |
1000 genomes | rs587777658 |
hgdp | rs587777658 |
ensembl | rs587777658 |
geneview | rs587777658 |
scholar | rs587777658 |
rs587777658 | |
pharmgkb | rs587777658 |
gwascentral | rs587777658 |
openSNP | rs587777658 |
23andMe | rs587777658 |
SNPshot | rs587777658 |
SNPdbe | rs587777658 |
MSV3d | rs587777658 |
GWAS Ctlg | rs587777658 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | Rs587777658(T;T) rs587777658(-;-) |
Alt | Rs587777658(T;T) rs587777658(-;-) |
Reference | Rs587777658(A;A) |
Significance | Pathogenic |
Disease | Marden Walker like syndrome |
Variation | info |
Gene | SCARF2 |
CLNDBN | Marden Walker like syndrome |
Reversed | 1 |
HGVS | NC_000022.10:g.20779735delT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000133556.3, |