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rs1057519732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519732(C;T)
Make rs1057519732(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66436824
GeneMAP2K1
is asnp
is mentioned by
dbSNPrs1057519732
dbSNP (old)rs1057519732
ClinGenrs1057519732
ebirs1057519732
HLIrs1057519732
Exacrs1057519732
Gnomadrs1057519732
Varsomers1057519732
Maprs1057519732
PheGenIrs1057519732
Biobankrs1057519732
1000 genomesrs1057519732
hgdprs1057519732
ensemblrs1057519732
gopubmedrs1057519732
geneviewrs1057519732
scholarrs1057519732
googlers1057519732
pharmgkbrs1057519732
gwascentralrs1057519732
openSNPrs1057519732
23andMers1057519732
23andMe allrs1057519732
SNPshotrs1057519732
SNPdbers1057519732
MSV3drs1057519732
GWAS Ctlgrs1057519732
Max Magnitude0
ClinVar
Risk rs1057519732(T;T)
Alt rs1057519732(T;T)
Reference Rs1057519732(C;C)
Significance Pathogenic
Disease Transitional cell carcinoma of the bladder Malignant melanoma Malignant neoplasm of body of uterus Malignant melanoma of skin Colorectal Neoplasms not provided
Variation info
Gene MAP2K1
CLNDBN Transitional cell carcinoma of the bladder Malignant melanoma Malignant neoplasm of body of uterus Malignant melanoma of skin Colorectal Neoplasms not provided
Reversed 0
HGVS NC_000015.9:g.66729162C>T
CLNSRC
CLNACC RCV000426713.1, RCV000433235.1, RCV000433927.1, RCV000443916.1, RCV000444865.1, RCV000482718.1,