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rs1060499961

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


Make rs1060499961(-;-)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position1207042
GeneSTK11
is asnp
is mentioned by
dbSNPrs1060499961
dbSNP (old)rs1060499961
ClinGenrs1060499961
ebirs1060499961
HLIrs1060499961
Exacrs1060499961
Gnomadrs1060499961
Varsomers1060499961
Maprs1060499961
PheGenIrs1060499961
Biobankrs1060499961
1000 genomesrs1060499961
hgdprs1060499961
ensemblrs1060499961
gopubmedrs1060499961
geneviewrs1060499961
scholarrs1060499961
googlers1060499961
pharmgkbrs1060499961
gwascentralrs1060499961
openSNPrs1060499961
23andMers1060499961
23andMe allrs1060499961
SNPshotrs1060499961
SNPdbers1060499961
MSV3drs1060499961
GWAS Ctlgrs1060499961
Max Magnitude5.8
ClinVar
Risk rs1060499961(-;-)
Alt rs1060499961(-;-)
Reference Rs1060499961(C;C)
Significance Pathogenic
Disease Peutz-Jeghers syndrome
Variation info
Gene STK11
CLNDBN Peutz-Jeghers syndrome
Reversed 0
HGVS NC_000019.9:g.1207041delC
CLNSRC
CLNACC RCV000466541.1,