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rs1057519908

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519908(G;G)
Make rs1057519908(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66435105
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519908
dbSNP (old)rs1057519908
ClinGenrs1057519908
ebirs1057519908
HLIrs1057519908
Exacrs1057519908
Gnomadrs1057519908
Varsomers1057519908
Maprs1057519908
PheGenIrs1057519908
Biobankrs1057519908
1000 genomesrs1057519908
hgdprs1057519908
ensemblrs1057519908
gopubmedrs1057519908
geneviewrs1057519908
scholarrs1057519908
googlers1057519908
pharmgkbrs1057519908
gwascentralrs1057519908
openSNPrs1057519908
23andMers1057519908
23andMe allrs1057519908
SNPshotrs1057519908
SNPdbers1057519908
MSV3drs1057519908
GWAS Ctlgrs1057519908
Max Magnitude0
ClinVar
Risk rs1057519908(G;G)
Alt rs1057519908(G;G)
Reference Rs1057519908(T;T)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms Malignant melanoma of skin Adenocarcinoma of lung Adenocarcinoma of stomach
Variation info
Gene MAP2K1
CLNDBN Colorectal Neoplasms Malignant melanoma of skin Adenocarcinoma of lung Adenocarcinoma of stomach
Reversed 0
HGVS NC_000015.9:g.66727443T>G
CLNSRC
CLNACC RCV000419468.1, RCV000430169.1, RCV000436917.1, RCV000440832.1,