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rs1057519728

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519728(C;C)
Make rs1057519728(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66435103
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519728
dbSNP (old)rs1057519728
ClinGenrs1057519728
ebirs1057519728
HLIrs1057519728
Exacrs1057519728
Gnomadrs1057519728
Varsomers1057519728
Maprs1057519728
PheGenIrs1057519728
Biobankrs1057519728
1000 genomesrs1057519728
hgdprs1057519728
ensemblrs1057519728
gopubmedrs1057519728
geneviewrs1057519728
scholarrs1057519728
googlers1057519728
pharmgkbrs1057519728
gwascentralrs1057519728
openSNPrs1057519728
23andMers1057519728
23andMe allrs1057519728
SNPshotrs1057519728
SNPdbers1057519728
MSV3drs1057519728
GWAS Ctlgrs1057519728
Max Magnitude0
ClinVar
Risk rs1057519728(A;A) rs1057519728(C;C) rs1057519728(G;G)
Alt rs1057519728(A;A) rs1057519728(C;C) rs1057519728(G;G)
Reference Rs1057519728(T;T)
Significance Pathogenic
Disease Colorectal Neoplasms Adenocarcinoma of lung Adenocarcinoma of stomach Malignant melanoma of skin Malignant melanoma
Variation info
Gene MAP2K1
CLNDBN Colorectal Neoplasms Adenocarcinoma of lung Adenocarcinoma of stomach Malignant melanoma of skin Malignant melanoma
Reversed 0
HGVS NC_000015.9:g.66727441T>A; NC_000015.9:g.66727441T>C; NC_000015.9:g.66727441T>G
CLNSRC
CLNACC RCV000421374.1, RCV000431446.1, RCV000432046.1, RCV000442281.1, RCV000435966.1, RCV000421852.1, RCV000422476.1, RCV000429056.1, RCV000439716.1,