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rs1057519805

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519805(C;C)
Make rs1057519805(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66436839
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519805
dbSNP (old)rs1057519805
ClinGenrs1057519805
ebirs1057519805
HLIrs1057519805
Exacrs1057519805
Gnomadrs1057519805
Varsomers1057519805
Maprs1057519805
PheGenIrs1057519805
Biobankrs1057519805
1000 genomesrs1057519805
hgdprs1057519805
ensemblrs1057519805
gopubmedrs1057519805
geneviewrs1057519805
scholarrs1057519805
googlers1057519805
pharmgkbrs1057519805
gwascentralrs1057519805
openSNPrs1057519805
23andMers1057519805
23andMe allrs1057519805
SNPshotrs1057519805
SNPdbers1057519805
MSV3drs1057519805
GWAS Ctlgrs1057519805
Max Magnitude0
ClinVar
Risk rs1057519805(C;C)
Alt rs1057519805(C;C)
Reference Rs1057519805(T;T)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene MAP2K1
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000015.9:g.66729177T>C
CLNSRC
CLNACC RCV000422377.1,