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rs1057519729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519729(A;C)
Make rs1057519729(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66435113
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519729
dbSNP (classic)rs1057519729
ClinGenrs1057519729
ebirs1057519729
HLIrs1057519729
Exacrs1057519729
Gnomadrs1057519729
Varsomers1057519729
LitVarrs1057519729
Maprs1057519729
PheGenIrs1057519729
Biobankrs1057519729
1000 genomesrs1057519729
hgdprs1057519729
ensemblrs1057519729
geneviewrs1057519729
scholarrs1057519729
googlers1057519729
pharmgkbrs1057519729
gwascentralrs1057519729
openSNPrs1057519729
23andMers1057519729
SNPshotrs1057519729
SNPdbers1057519729
MSV3drs1057519729
GWAS Ctlgrs1057519729
Max Magnitude0
ClinVar
Risk rs1057519729(C;C)
Alt rs1057519729(C;C)
Reference Rs1057519729(A;A)
Significance Pathogenic
Disease Non-small cell lung cancer Malignant melanoma
Variation info
Gene MAP2K1
CLNDBN Non-small cell lung cancer Malignant melanoma
Reversed 0
HGVS NC_000015.9:g.66727451A>C
CLNSRC
CLNACC RCV000418731.1, RCV000429601.1,