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rs1057519808

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519808(A;C)
Make rs1057519808(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position4117543
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs1057519808
dbSNP (old)rs1057519808
ClinGenrs1057519808
ebirs1057519808
HLIrs1057519808
Exacrs1057519808
Gnomadrs1057519808
Varsomers1057519808
Maprs1057519808
PheGenIrs1057519808
Biobankrs1057519808
1000 genomesrs1057519808
hgdprs1057519808
ensemblrs1057519808
gopubmedrs1057519808
geneviewrs1057519808
scholarrs1057519808
googlers1057519808
pharmgkbrs1057519808
gwascentralrs1057519808
openSNPrs1057519808
23andMers1057519808
23andMe allrs1057519808
SNPshotrs1057519808
SNPdbers1057519808
MSV3drs1057519808
GWAS Ctlgrs1057519808
Max Magnitude0
ClinVar
Risk rs1057519808(C;C)
Alt rs1057519808(C;C)
Reference Rs1057519808(A;A)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene MAP2K2
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000019.9:g.4117541T>G
CLNSRC
CLNACC RCV000421323.1,