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rs1057519819

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519819(C;C)
Make rs1057519819(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66436750
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519819
dbSNP (old)rs1057519819
ClinGenrs1057519819
ebirs1057519819
HLIrs1057519819
Exacrs1057519819
Gnomadrs1057519819
Varsomers1057519819
Maprs1057519819
PheGenIrs1057519819
Biobankrs1057519819
1000 genomesrs1057519819
hgdprs1057519819
ensemblrs1057519819
gopubmedrs1057519819
geneviewrs1057519819
scholarrs1057519819
googlers1057519819
pharmgkbrs1057519819
gwascentralrs1057519819
openSNPrs1057519819
23andMers1057519819
23andMe allrs1057519819
SNPshotrs1057519819
SNPdbers1057519819
MSV3drs1057519819
GWAS Ctlgrs1057519819
Max Magnitude0
ClinVar
Risk rs1057519819(C;C)
Alt rs1057519819(C;C)
Reference Rs1057519819(T;T)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene MAP2K1
CLNDBN Neoplasm
Reversed 0
HGVS NC_000015.9:g.66729088T>C
CLNSRC
CLNACC RCV000420695.1,