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rs1064794805

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 5.8 STK11 gene mutation associated with Peutz-Jeghers syndrome
Chromosome19
Position1220435
GeneSTK11
is asnp
is mentioned by
dbSNPrs1064794805
dbSNP (old)rs1064794805
ClinGenrs1064794805
ebirs1064794805
HLIrs1064794805
Exacrs1064794805
Gnomadrs1064794805
Varsomers1064794805
Maprs1064794805
PheGenIrs1064794805
Biobankrs1064794805
1000 genomesrs1064794805
hgdprs1064794805
ensemblrs1064794805
gopubmedrs1064794805
geneviewrs1064794805
scholarrs1064794805
googlers1064794805
pharmgkbrs1064794805
gwascentralrs1064794805
openSNPrs1064794805
23andMers1064794805
23andMe allrs1064794805
SNPshotrs1064794805
SNPdbers1064794805
MSV3drs1064794805
GWAS Ctlgrs1064794805
Max Magnitude5.8
ClinVar
Risk rs1064794805(G;G)
Alt rs1064794805(G;G)
Reference Rs1064794805(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STK11
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.1220434A>G
CLNSRC
CLNACC RCV000482078.1,