Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520606

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
Make rs1057520606(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1221244
GeneSTK11
is asnp
is mentioned by
dbSNPrs1057520606
dbSNP (classic)rs1057520606
ClinGenrs1057520606
ebirs1057520606
HLIrs1057520606
Exacrs1057520606
Gnomadrs1057520606
Varsomers1057520606
LitVarrs1057520606
Maprs1057520606
PheGenIrs1057520606
Biobankrs1057520606
1000 genomesrs1057520606
hgdprs1057520606
ensemblrs1057520606
geneviewrs1057520606
scholarrs1057520606
googlers1057520606
pharmgkbrs1057520606
gwascentralrs1057520606
openSNPrs1057520606
23andMers1057520606
23andMe allrs1057520606
SNPshotrs1057520606
SNPdbers1057520606
MSV3drs1057520606
GWAS Ctlgrs1057520606
Max Magnitude5.8
ClinVar
Risk rs1057520606(T;T)
Alt rs1057520606(T;T)
Reference Rs1057520606(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STK11
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.1221243G>T
CLNSRC
CLNACC RCV000423599.1,