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rs1057519730

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519730(G;G)
Make rs1057519730(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66436786
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519730
dbSNP (old)rs1057519730
ClinGenrs1057519730
ebirs1057519730
HLIrs1057519730
Exacrs1057519730
Gnomadrs1057519730
Varsomers1057519730
Maprs1057519730
PheGenIrs1057519730
Biobankrs1057519730
1000 genomesrs1057519730
hgdprs1057519730
ensemblrs1057519730
gopubmedrs1057519730
geneviewrs1057519730
scholarrs1057519730
googlers1057519730
pharmgkbrs1057519730
gwascentralrs1057519730
openSNPrs1057519730
23andMers1057519730
23andMe allrs1057519730
SNPshotrs1057519730
SNPdbers1057519730
MSV3drs1057519730
GWAS Ctlgrs1057519730
Max Magnitude0
ClinVar
Risk rs1057519730(A;A) rs1057519730(G;G)
Alt rs1057519730(A;A) rs1057519730(G;G)
Reference Rs1057519730(T;T)
Significance Pathogenic
Disease Neoplasm Malignant melanoma
Variation info
Gene MAP2K1
CLNDBN Neoplasm Malignant melanoma
Reversed 0
HGVS NC_000015.9:g.66729124T>A; NC_000015.9:g.66729124T>G
CLNSRC
CLNACC RCV000440339.1, RCV000434378.1,