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rs1064796831

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;CC) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
(CC;CC) 0 common in clinvar
Chromosome19
Position1221319
GeneSTK11
is asnp
is mentioned by
dbSNPrs1064796831
dbSNP (old)rs1064796831
ClinGenrs1064796831
ebirs1064796831
HLIrs1064796831
Exacrs1064796831
Gnomadrs1064796831
Varsomers1064796831
Maprs1064796831
PheGenIrs1064796831
Biobankrs1064796831
1000 genomesrs1064796831
hgdprs1064796831
ensemblrs1064796831
gopubmedrs1064796831
geneviewrs1064796831
scholarrs1064796831
googlers1064796831
pharmgkbrs1064796831
gwascentralrs1064796831
openSNPrs1064796831
23andMers1064796831
23andMe allrs1064796831
SNPshotrs1064796831
SNPdbers1064796831
MSV3drs1064796831
GWAS Ctlgrs1064796831
Max Magnitude5.8
ClinVar
Risk rs1064796831(-;-)
Alt rs1064796831(-;-)
Reference Rs1064796831(CC;CC)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene STK11
CLNDBN not specified not provided
Reversed 0
HGVS NC_000019.9:g.1221318_1221319delCC
CLNSRC
CLNACC RCV000221464.1, RCV000485596.1,