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rs1057519810

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519810(A;A)
Make rs1057519810(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position4117619
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs1057519810
dbSNP (old)rs1057519810
ClinGenrs1057519810
ebirs1057519810
HLIrs1057519810
Exacrs1057519810
Gnomadrs1057519810
Varsomers1057519810
LitVarrs1057519810
Maprs1057519810
PheGenIrs1057519810
Biobankrs1057519810
1000 genomesrs1057519810
hgdprs1057519810
ensemblrs1057519810
gopubmedrs1057519810
geneviewrs1057519810
scholarrs1057519810
googlers1057519810
pharmgkbrs1057519810
gwascentralrs1057519810
openSNPrs1057519810
23andMers1057519810
23andMe allrs1057519810
SNPshotrs1057519810
SNPdbers1057519810
MSV3drs1057519810
GWAS Ctlgrs1057519810
Max Magnitude0
ClinVar
Risk rs1057519810(A;A)
Alt rs1057519810(A;A)
Reference Rs1057519810(G;G)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene MAP2K2
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000019.9:g.4117617C>T
CLNSRC
CLNACC RCV000444084.1,