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rs869025339

From SNPedia

Orientationplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs869025339(-;-)
Make rs869025339(-;AAG)
Make rs869025339(AAG;AAG)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position66435121
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs869025339
ebirs869025339
HLIrs869025339
Exacrs869025339
Varsomers869025339
Maprs869025339
PheGenIrs869025339
hapmaprs869025339
1000 genomesrs869025339
hgdprs869025339
ensemblrs869025339
gopubmedrs869025339
geneviewrs869025339
scholarrs869025339
googlers869025339
pharmgkbrs869025339
gwascentralrs869025339
openSNPrs869025339
23andMers869025339
23andMe allrs869025339
SNP Nexus

SNPshotrs869025339
SNPdbers869025339
MSV3drs869025339
GWAS Ctlgrs869025339
Max Magnitude0
ClinVar
Risk rs869025339(;)
Alt rs869025339(;)
Reference rs869025339(AGA;AGA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAP2K1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.66727459_66727461delAAG
CLNSRC
CLNACC RCV000207500.1,