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rs1057519910

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519910(G;G)
Make rs1057519910(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position4117551
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs1057519910
dbSNP (old)rs1057519910
ClinGenrs1057519910
ebirs1057519910
HLIrs1057519910
Exacrs1057519910
Gnomadrs1057519910
Varsomers1057519910
Maprs1057519910
PheGenIrs1057519910
Biobankrs1057519910
1000 genomesrs1057519910
hgdprs1057519910
ensemblrs1057519910
gopubmedrs1057519910
geneviewrs1057519910
scholarrs1057519910
googlers1057519910
pharmgkbrs1057519910
gwascentralrs1057519910
openSNPrs1057519910
23andMers1057519910
23andMe allrs1057519910
SNPshotrs1057519910
SNPdbers1057519910
MSV3drs1057519910
GWAS Ctlgrs1057519910
Max Magnitude0
ClinVar
Risk rs1057519910(G;G)
Alt rs1057519910(G;G)
Reference Rs1057519910(T;T)
Significance Probable-Pathogenic
Disease Malignant melanoma of skin Pancreatic adenocarcinoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach
Variation info
Gene MAP2K2
CLNDBN Malignant melanoma of skin Pancreatic adenocarcinoma Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach
Reversed 1
HGVS NC_000019.9:g.4117549A>C
CLNSRC
CLNACC RCV000417753.1, RCV000428429.1, RCV000429600.1, RCV000438529.1,