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rs1057519820

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519820(A;C)
Make rs1057519820(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66436810
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519820
dbSNP (old)rs1057519820
ClinGenrs1057519820
ebirs1057519820
HLIrs1057519820
Exacrs1057519820
Gnomadrs1057519820
Varsomers1057519820
LitVarrs1057519820
Maprs1057519820
PheGenIrs1057519820
Biobankrs1057519820
1000 genomesrs1057519820
hgdprs1057519820
ensemblrs1057519820
gopubmedrs1057519820
geneviewrs1057519820
scholarrs1057519820
googlers1057519820
pharmgkbrs1057519820
gwascentralrs1057519820
openSNPrs1057519820
23andMers1057519820
23andMe allrs1057519820
SNPshotrs1057519820
SNPdbers1057519820
MSV3drs1057519820
GWAS Ctlgrs1057519820
Max Magnitude0
ClinVar
Risk rs1057519820(C;C)
Alt rs1057519820(C;C)
Reference Rs1057519820(A;A)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene MAP2K1
CLNDBN Neoplasm
Reversed 0
HGVS NC_000015.9:g.66729148A>C
CLNSRC
CLNACC RCV000423068.1,