rs1131690922
From SNPedia
Orientation | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common/normal |
(-;ACCT) | 5.8 | STK11 gene mutation associated with Peutz-Jeghers syndrome |
Make rs1131690922(ACCT;ACCT) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 1220408 |
Gene | STK11 |
is a | snp |
is | mentioned by |
dbSNP | rs1131690922 |
dbSNP (classic) | rs1131690922 |
ClinGen | rs1131690922 |
ebi | rs1131690922 |
HLI | rs1131690922 |
Exac | rs1131690922 |
Gnomad | rs1131690922 |
Varsome | rs1131690922 |
LitVar | rs1131690922 |
Map | rs1131690922 |
PheGenI | rs1131690922 |
Biobank | rs1131690922 |
1000 genomes | rs1131690922 |
hgdp | rs1131690922 |
ensembl | rs1131690922 |
geneview | rs1131690922 |
scholar | rs1131690922 |
rs1131690922 | |
pharmgkb | rs1131690922 |
gwascentral | rs1131690922 |
openSNP | rs1131690922 |
23andMe | rs1131690922 |
SNPshot | rs1131690922 |
SNPdbe | rs1131690922 |
MSV3d | rs1131690922 |
GWAS Ctlg | rs1131690922 |
Max Magnitude | 5.8 |