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rs1057519822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519822(A;A)
Make rs1057519822(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66481818
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519822
dbSNP (old)rs1057519822
ClinGenrs1057519822
ebirs1057519822
HLIrs1057519822
Exacrs1057519822
Gnomadrs1057519822
Varsomers1057519822
Maprs1057519822
PheGenIrs1057519822
Biobankrs1057519822
1000 genomesrs1057519822
hgdprs1057519822
ensemblrs1057519822
gopubmedrs1057519822
geneviewrs1057519822
scholarrs1057519822
googlers1057519822
pharmgkbrs1057519822
gwascentralrs1057519822
openSNPrs1057519822
23andMers1057519822
23andMe allrs1057519822
SNPshotrs1057519822
SNPdbers1057519822
MSV3drs1057519822
GWAS Ctlgrs1057519822
Max Magnitude0
ClinVar
Risk rs1057519822(A;A)
Alt rs1057519822(A;A)
Reference Rs1057519822(T;T)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene MAP2K1
CLNDBN Neoplasm
Reversed 0
HGVS NC_000015.9:g.66774156T>A
CLNSRC
CLNACC RCV000422017.1,