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rs1057519812

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519812(C;C)
Make rs1057519812(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54277977
GenePDGFRA
is asnp
is mentioned by
dbSNPrs1057519812
dbSNP (old)rs1057519812
ClinGenrs1057519812
ebirs1057519812
HLIrs1057519812
Exacrs1057519812
Gnomadrs1057519812
Varsomers1057519812
Maprs1057519812
PheGenIrs1057519812
Biobankrs1057519812
1000 genomesrs1057519812
hgdprs1057519812
ensemblrs1057519812
gopubmedrs1057519812
geneviewrs1057519812
scholarrs1057519812
googlers1057519812
pharmgkbrs1057519812
gwascentralrs1057519812
openSNPrs1057519812
23andMers1057519812
23andMe allrs1057519812
SNPshotrs1057519812
SNPdbers1057519812
MSV3drs1057519812
GWAS Ctlgrs1057519812
Max Magnitude0
ClinVar
Risk rs1057519812(C;C)
Alt rs1057519812(C;C)
Reference Rs1057519812(T;T)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene PDGFRA
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000004.11:g.55144144T>C
CLNSRC
CLNACC RCV000434301.1,