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rs1057517830

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(G;G) 0 common in clinvar


Make rs1057517830(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1221212
GeneSTK11
is asnp
is mentioned by
dbSNPrs1057517830
dbSNP (old)rs1057517830
ClinGenrs1057517830
ebirs1057517830
HLIrs1057517830
Exacrs1057517830
Gnomadrs1057517830
Varsomers1057517830
Maprs1057517830
PheGenIrs1057517830
Biobankrs1057517830
1000 genomesrs1057517830
hgdprs1057517830
ensemblrs1057517830
gopubmedrs1057517830
geneviewrs1057517830
scholarrs1057517830
googlers1057517830
pharmgkbrs1057517830
gwascentralrs1057517830
openSNPrs1057517830
23andMers1057517830
23andMe allrs1057517830
SNPshotrs1057517830
SNPdbers1057517830
MSV3drs1057517830
GWAS Ctlgrs1057517830
Max Magnitude5.8
ClinVar
Risk rs1057517830(A;A)
Alt rs1057517830(A;A)
Reference Rs1057517830(G;G)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene STK11
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000019.9:g.1221211G>A
CLNSRC
CLNACC RCV000413399.1, RCV000492178.1,