rs2075702
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs2075702(C;C) |
Make rs2075702(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31969734 |
Gene | DXO, SKIV2L, STK19 |
is a | snp |
is | mentioned by |
dbSNP | rs2075702 |
dbSNP (classic) | rs2075702 |
ClinGen | rs2075702 |
ebi | rs2075702 |
HLI | rs2075702 |
Exac | rs2075702 |
Gnomad | rs2075702 |
Varsome | rs2075702 |
LitVar | rs2075702 |
Map | rs2075702 |
PheGenI | rs2075702 |
Biobank | rs2075702 |
1000 genomes | rs2075702 |
hgdp | rs2075702 |
ensembl | rs2075702 |
geneview | rs2075702 |
scholar | rs2075702 |
rs2075702 | |
pharmgkb | rs2075702 |
gwascentral | rs2075702 |
openSNP | rs2075702 |
23andMe | rs2075702 |
SNPshot | rs2075702 |
SNPdbe | rs2075702 |
MSV3d | rs2075702 |
GWAS Ctlg | rs2075702 |
GMAF | 0.01056 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19556007] Role of RDBP and SKIV2L variants in the major histocompatibility complex class III region in polypoidal choroidal vasculopathy etiology
ClinVar | |
---|---|
Risk | rs2075702(C;C) |
Alt | rs2075702(C;C) |
Reference | Rs2075702(T;T) |
Significance | Probable-non-pathogenic |
Disease | Trichohepatoenteric syndrome |
Variation | info |
Gene | DXO STK19 SKIV2L |
CLNDBN | Trichohepatoenteric syndrome |
Reversed | 0 |
HGVS | NC_000006.11:g.31937511T>C |
CLNSRC | |
CLNACC | RCV000294596.1, |