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rs1057519786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519786(C;G)
Make rs1057519786(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position47566722
GeneARAF
is asnp
is mentioned by
dbSNPrs1057519786
dbSNP (old)rs1057519786
ClinGenrs1057519786
ebirs1057519786
HLIrs1057519786
Exacrs1057519786
Gnomadrs1057519786
Varsomers1057519786
Maprs1057519786
PheGenIrs1057519786
Biobankrs1057519786
1000 genomesrs1057519786
hgdprs1057519786
ensemblrs1057519786
gopubmedrs1057519786
geneviewrs1057519786
scholarrs1057519786
googlers1057519786
pharmgkbrs1057519786
gwascentralrs1057519786
openSNPrs1057519786
23andMers1057519786
23andMe allrs1057519786
SNPshotrs1057519786
SNPdbers1057519786
MSV3drs1057519786
GWAS Ctlgrs1057519786
Max Magnitude0
ClinVar
Risk rs1057519786(G;G) rs1057519786(T;T)
Alt rs1057519786(G;G) rs1057519786(T;T)
Reference Rs1057519786(C;C)
Significance Probable-Pathogenic
Disease Non-small cell lung cancer Malignant melanoma of skin Papillary renal cell carcinoma Adenocarcinoma of lung
Variation info
Gene ARAF
CLNDBN Non-small cell lung cancer Malignant melanoma of skin Papillary renal cell carcinoma, sporadic Adenocarcinoma of lung
Reversed 0
HGVS NC_000023.10:g.47426121C>G; NC_000023.10:g.47426121C>T
CLNSRC
CLNACC RCV000419218.1, RCV000427514.1, RCV000430187.1, RCV000436910.1, RCV000417875.1, RCV000429142.1, RCV000435898.1,