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rs1057520040

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520040(A;G)
Make rs1057520040(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1218449
GeneSTK11
is asnp
is mentioned by
dbSNPrs1057520040
dbSNP (classic)rs1057520040
ClinGenrs1057520040
ebirs1057520040
HLIrs1057520040
Exacrs1057520040
Gnomadrs1057520040
Varsomers1057520040
LitVarrs1057520040
Maprs1057520040
PheGenIrs1057520040
Biobankrs1057520040
1000 genomesrs1057520040
hgdprs1057520040
ensemblrs1057520040
geneviewrs1057520040
scholarrs1057520040
googlers1057520040
pharmgkbrs1057520040
gwascentralrs1057520040
openSNPrs1057520040
23andMers1057520040
23andMe allrs1057520040
SNPshotrs1057520040
SNPdbers1057520040
MSV3drs1057520040
GWAS Ctlgrs1057520040
Max Magnitude0
ClinVar
Risk rs1057520040(G;G)
Alt rs1057520040(G;G)
Reference Rs1057520040(A;A)
Significance Probable-Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1218448A>G
CLNSRC
CLNACC RCV000434992.1,