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rs1057519823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519823(C;C)
Make rs1057519823(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66481830
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519823
dbSNP (classic)rs1057519823
ClinGenrs1057519823
ebirs1057519823
HLIrs1057519823
Exacrs1057519823
Gnomadrs1057519823
Varsomers1057519823
LitVarrs1057519823
Maprs1057519823
PheGenIrs1057519823
Biobankrs1057519823
1000 genomesrs1057519823
hgdprs1057519823
ensemblrs1057519823
geneviewrs1057519823
scholarrs1057519823
googlers1057519823
pharmgkbrs1057519823
gwascentralrs1057519823
openSNPrs1057519823
23andMers1057519823
23andMe allrs1057519823
SNPshotrs1057519823
SNPdbers1057519823
MSV3drs1057519823
GWAS Ctlgrs1057519823
Max Magnitude0
ClinVar
Risk rs1057519823(C;C)
Alt rs1057519823(C;C)
Reference Rs1057519823(T;T)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene MAP2K1
CLNDBN Neoplasm
Reversed 0
HGVS NC_000015.9:g.66774168T>C
CLNSRC
CLNACC RCV000432883.1,