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rs1057519909

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519909(A;C)
Make rs1057519909(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66435116
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519909
dbSNP (classic)rs1057519909
ClinGenrs1057519909
ebirs1057519909
HLIrs1057519909
Exacrs1057519909
Gnomadrs1057519909
Varsomers1057519909
LitVarrs1057519909
Maprs1057519909
PheGenIrs1057519909
Biobankrs1057519909
1000 genomesrs1057519909
hgdprs1057519909
ensemblrs1057519909
geneviewrs1057519909
scholarrs1057519909
googlers1057519909
pharmgkbrs1057519909
gwascentralrs1057519909
openSNPrs1057519909
23andMers1057519909
23andMe allrs1057519909
SNPshotrs1057519909
SNPdbers1057519909
MSV3drs1057519909
GWAS Ctlgrs1057519909
Max Magnitude0
ClinVar
Risk rs1057519909(C;C)
Alt rs1057519909(C;C)
Reference Rs1057519909(A;A)
Significance Probable-Pathogenic
Disease Squamous cell carcinoma of the head and neck Malignant melanoma of skin Malignant lymphoma Adenocarcinoma of stomach Adenocarcinoma of prostate Adenocarcinoma of lung
Variation info
Gene MAP2K1
CLNDBN Squamous cell carcinoma of the head and neck Malignant melanoma of skin Malignant lymphoma, non-Hodgkin Adenocarcinoma of stomach Adenocarcinoma of prostate Adenocarcinoma of lung
Reversed 0
HGVS NC_000015.9:g.66727454A>C
CLNSRC
CLNACC RCV000426154.1, RCV000427226.1, RCV000436846.1, RCV000437934.1, RCV000442142.1, RCV000444739.1,