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rs876661012

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876661012(-;-)
Make rs876661012(-;A)
Make rs876661012(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position1207092
GeneSTK11
is asnp
is mentioned by
dbSNPrs876661012
ebirs876661012
HLIrs876661012
Exacrs876661012
Varsomers876661012
Maprs876661012
PheGenIrs876661012
hapmaprs876661012
1000 genomesrs876661012
hgdprs876661012
ensemblrs876661012
gopubmedrs876661012
geneviewrs876661012
scholarrs876661012
googlers876661012
pharmgkbrs876661012
gwascentralrs876661012
openSNPrs876661012
23andMers876661012
23andMe allrs876661012
SNP Nexus

SNPshotrs876661012
SNPdbers876661012
MSV3drs876661012
GWAS Ctlgrs876661012
Max Magnitude0
ClinVar
Risk rs876661012(A;A)
Alt rs876661012(A;A)
Reference rs876661012(;)
Significance Pathogenic
Disease not provided
Variation info
Gene STK11
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.1207091dupA
CLNSRC
CLNACC RCV000216923.1,