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

rs1057520038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520038(A;A)
Make rs1057520038(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1220627
GeneSTK11
is asnp
is mentioned by
dbSNPrs1057520038
dbSNP (classic)rs1057520038
ClinGenrs1057520038
ebirs1057520038
HLIrs1057520038
Exacrs1057520038
Gnomadrs1057520038
Varsomers1057520038
LitVarrs1057520038
Maprs1057520038
PheGenIrs1057520038
Biobankrs1057520038
1000 genomesrs1057520038
hgdprs1057520038
ensemblrs1057520038
geneviewrs1057520038
scholarrs1057520038
googlers1057520038
pharmgkbrs1057520038
gwascentralrs1057520038
openSNPrs1057520038
23andMers1057520038
23andMe allrs1057520038
SNPshotrs1057520038
SNPdbers1057520038
MSV3drs1057520038
GWAS Ctlgrs1057520038
Max Magnitude0
ClinVar
Risk rs1057520038(A;A)
Alt rs1057520038(A;A)
Reference Rs1057520038(G;G)
Significance Probable-Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1220626G>A
CLNSRC
CLNACC RCV000427128.1,