rs775341740
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs775341740(A;A) |
Make rs775341740(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 148118565 |
Gene | SPINK5 |
is a | snp |
is | mentioned by |
dbSNP | rs775341740 |
dbSNP (classic) | rs775341740 |
ClinGen | rs775341740 |
ebi | rs775341740 |
HLI | rs775341740 |
Exac | rs775341740 |
Gnomad | rs775341740 |
Varsome | rs775341740 |
LitVar | rs775341740 |
Map | rs775341740 |
PheGenI | rs775341740 |
Biobank | rs775341740 |
1000 genomes | rs775341740 |
hgdp | rs775341740 |
ensembl | rs775341740 |
geneview | rs775341740 |
scholar | rs775341740 |
rs775341740 | |
pharmgkb | rs775341740 |
gwascentral | rs775341740 |
openSNP | rs775341740 |
23andMe | rs775341740 |
SNPshot | rs775341740 |
SNPdbe | rs775341740 |
MSV3d | rs775341740 |
GWAS Ctlg | rs775341740 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775341740(A;A) |
Alt | rs775341740(A;A) |
Reference | Rs775341740(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SPINK5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.147498128G>A |
CLNSRC | |
CLNACC | RCV000413096.1, |