rs886039372
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs886039372(-;-) |
Make rs886039372(-;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 11 |
Position | 86952468 |
Gene | FZD4, PRSS23 |
is a | snp |
is | mentioned by |
dbSNP | rs886039372 |
dbSNP (classic) | rs886039372 |
ClinGen | rs886039372 |
ebi | rs886039372 |
HLI | rs886039372 |
Exac | rs886039372 |
Gnomad | rs886039372 |
Varsome | rs886039372 |
LitVar | rs886039372 |
Map | rs886039372 |
PheGenI | rs886039372 |
Biobank | rs886039372 |
1000 genomes | rs886039372 |
hgdp | rs886039372 |
ensembl | rs886039372 |
geneview | rs886039372 |
scholar | rs886039372 |
rs886039372 | |
pharmgkb | rs886039372 |
gwascentral | rs886039372 |
openSNP | rs886039372 |
23andMe | rs886039372 |
SNPshot | rs886039372 |
SNPdbe | rs886039372 |
MSV3d | rs886039372 |
GWAS Ctlg | rs886039372 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886039372(-;-) |
Alt | rs886039372(-;-) |
Reference | Rs886039372(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | PRSS23 FZD4 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000011.9:g.86663510delG |
CLNSRC | |
CLNACC | RCV000254871.1, |