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rs1057519806

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519806(A;G)
Make rs1057519806(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position4110583
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs1057519806
dbSNP (old)rs1057519806
ClinGenrs1057519806
ebirs1057519806
HLIrs1057519806
Exacrs1057519806
Gnomadrs1057519806
Varsomers1057519806
LitVarrs1057519806
Maprs1057519806
PheGenIrs1057519806
Biobankrs1057519806
1000 genomesrs1057519806
hgdprs1057519806
ensemblrs1057519806
gopubmedrs1057519806
geneviewrs1057519806
scholarrs1057519806
googlers1057519806
pharmgkbrs1057519806
gwascentralrs1057519806
openSNPrs1057519806
23andMers1057519806
23andMe allrs1057519806
SNPshotrs1057519806
SNPdbers1057519806
MSV3drs1057519806
GWAS Ctlgrs1057519806
Max Magnitude0
ClinVar
Risk rs1057519806(G;G)
Alt rs1057519806(G;G)
Reference Rs1057519806(A;A)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene MAP2K2
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000019.9:g.4110581T>C
CLNSRC
CLNACC RCV000429584.1,