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rs1057519807

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519807(A;A)
Make rs1057519807(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position4110586
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs1057519807
dbSNP (old)rs1057519807
ClinGenrs1057519807
ebirs1057519807
HLIrs1057519807
Exacrs1057519807
Gnomadrs1057519807
Varsomers1057519807
Maprs1057519807
PheGenIrs1057519807
Biobankrs1057519807
1000 genomesrs1057519807
hgdprs1057519807
ensemblrs1057519807
gopubmedrs1057519807
geneviewrs1057519807
scholarrs1057519807
googlers1057519807
pharmgkbrs1057519807
gwascentralrs1057519807
openSNPrs1057519807
23andMers1057519807
23andMe allrs1057519807
SNPshotrs1057519807
SNPdbers1057519807
MSV3drs1057519807
GWAS Ctlgrs1057519807
Max Magnitude0
ClinVar
Risk rs1057519807(A;A)
Alt rs1057519807(A;A)
Reference Rs1057519807(T;T)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene MAP2K2
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000019.9:g.4110584A>T
CLNSRC
CLNACC RCV000438500.1,