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rs886041310

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome19
Position4117539
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs886041310
dbSNP (classic)rs886041310
ClinGenrs886041310
ebirs886041310
HLIrs886041310
Exacrs886041310
Gnomadrs886041310
Varsomers886041310
LitVarrs886041310
Maprs886041310
PheGenIrs886041310
Biobankrs886041310
1000 genomesrs886041310
hgdprs886041310
ensemblrs886041310
geneviewrs886041310
scholarrs886041310
googlers886041310
pharmgkbrs886041310
gwascentralrs886041310
openSNPrs886041310
23andMers886041310
23andMe allrs886041310
SNPshotrs886041310
SNPdbers886041310
MSV3drs886041310
GWAS Ctlgrs886041310
Max Magnitude0
ClinVar
Risk rs886041310(C;C)
Alt rs886041310(C;C)
Reference Rs886041310(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAP2K2
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.4117537T>G
CLNSRC
CLNACC RCV000330980.1,