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rs1057519876

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519876(G;G)
Make rs1057519876(G;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position47566721
GeneARAF
is asnp
is mentioned by
dbSNPrs1057519876
dbSNP (old)rs1057519876
ClinGenrs1057519876
ebirs1057519876
HLIrs1057519876
Exacrs1057519876
Gnomadrs1057519876
Varsomers1057519876
Maprs1057519876
PheGenIrs1057519876
Biobankrs1057519876
1000 genomesrs1057519876
hgdprs1057519876
ensemblrs1057519876
gopubmedrs1057519876
geneviewrs1057519876
scholarrs1057519876
googlers1057519876
pharmgkbrs1057519876
gwascentralrs1057519876
openSNPrs1057519876
23andMers1057519876
23andMe allrs1057519876
SNPshotrs1057519876
SNPdbers1057519876
MSV3drs1057519876
GWAS Ctlgrs1057519876
Max Magnitude0
ClinVar
Risk rs1057519876(G;G)
Alt rs1057519876(G;G)
Reference Rs1057519876(T;T)
Significance Probable-Pathogenic
Disease Papillary renal cell carcinoma Adenocarcinoma of lung Malignant melanoma of skin
Variation info
Gene ARAF
CLNDBN Papillary renal cell carcinoma, sporadic Adenocarcinoma of lung Malignant melanoma of skin
Reversed 0
HGVS NC_000023.10:g.47426120T>G
CLNSRC
CLNACC RCV000421117.1, RCV000428557.1, RCV000438348.1,