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rs1057519821

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519821(C;C)
Make rs1057519821(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66436814
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519821
dbSNP (old)rs1057519821
ClinGenrs1057519821
ebirs1057519821
HLIrs1057519821
Exacrs1057519821
Gnomadrs1057519821
Varsomers1057519821
Maprs1057519821
PheGenIrs1057519821
Biobankrs1057519821
1000 genomesrs1057519821
hgdprs1057519821
ensemblrs1057519821
gopubmedrs1057519821
geneviewrs1057519821
scholarrs1057519821
googlers1057519821
pharmgkbrs1057519821
gwascentralrs1057519821
openSNPrs1057519821
23andMers1057519821
23andMe allrs1057519821
SNPshotrs1057519821
SNPdbers1057519821
MSV3drs1057519821
GWAS Ctlgrs1057519821
Max Magnitude0
ClinVar
Risk rs1057519821(C;C) rs1057519821(T;T)
Alt rs1057519821(C;C) rs1057519821(T;T)
Reference Rs1057519821(G;G)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene MAP2K1
CLNDBN Neoplasm
Reversed 0
HGVS NC_000015.9:g.66729152G>C; NC_000015.9:g.66729152G>T
CLNSRC
CLNACC RCV000433785.1, RCV000439225.1,