rs387906795
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs387906795(G;T) |
Make rs387906795(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 20086175 |
Gene | PLA2G5 |
is a | snp |
is | mentioned by |
dbSNP | rs387906795 |
dbSNP (classic) | rs387906795 |
ClinGen | rs387906795 |
ebi | rs387906795 |
HLI | rs387906795 |
Exac | rs387906795 |
Gnomad | rs387906795 |
Varsome | rs387906795 |
LitVar | rs387906795 |
Map | rs387906795 |
PheGenI | rs387906795 |
Biobank | rs387906795 |
1000 genomes | rs387906795 |
hgdp | rs387906795 |
ensembl | rs387906795 |
geneview | rs387906795 |
scholar | rs387906795 |
rs387906795 | |
pharmgkb | rs387906795 |
gwascentral | rs387906795 |
openSNP | rs387906795 |
23andMe | rs387906795 |
SNPshot | rs387906795 |
SNPdbe | rs387906795 |
MSV3d | rs387906795 |
GWAS Ctlg | rs387906795 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906795(A;A) rs387906795(T;T) |
Alt | rs387906795(A;A) rs387906795(T;T) |
Reference | Rs387906795(G;G) |
Significance | Other |
Disease | Fleck retina |
Variation | info |
Gene | PLA2G5 |
CLNDBN | Fleck retina, familial benign |
Reversed | 0 |
HGVS | NC_000001.10:g.20412668G>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000023076.3, |