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rs1057519734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519734(C;T)
Make rs1057519734(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66485086
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519734
dbSNP (old)rs1057519734
ClinGenrs1057519734
ebirs1057519734
HLIrs1057519734
Exacrs1057519734
Gnomadrs1057519734
Varsomers1057519734
Maprs1057519734
PheGenIrs1057519734
Biobankrs1057519734
1000 genomesrs1057519734
hgdprs1057519734
ensemblrs1057519734
gopubmedrs1057519734
geneviewrs1057519734
scholarrs1057519734
googlers1057519734
pharmgkbrs1057519734
gwascentralrs1057519734
openSNPrs1057519734
23andMers1057519734
23andMe allrs1057519734
SNPshotrs1057519734
SNPdbers1057519734
MSV3drs1057519734
GWAS Ctlgrs1057519734
Max Magnitude0
ClinVar
Risk rs1057519734(T;T)
Alt rs1057519734(T;T)
Reference Rs1057519734(C;C)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene MAP2K1
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000015.9:g.66777424C>T
CLNSRC
CLNACC RCV000430494.1,