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rs1057519813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519813(A;A)
Make rs1057519813(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54285923
GenePDGFRA
is asnp
is mentioned by
dbSNPrs1057519813
dbSNP (old)rs1057519813
ClinGenrs1057519813
ebirs1057519813
HLIrs1057519813
Exacrs1057519813
Gnomadrs1057519813
Varsomers1057519813
LitVarrs1057519813
Maprs1057519813
PheGenIrs1057519813
Biobankrs1057519813
1000 genomesrs1057519813
hgdprs1057519813
ensemblrs1057519813
gopubmedrs1057519813
geneviewrs1057519813
scholarrs1057519813
googlers1057519813
pharmgkbrs1057519813
gwascentralrs1057519813
openSNPrs1057519813
23andMers1057519813
23andMe allrs1057519813
SNPshotrs1057519813
SNPdbers1057519813
MSV3drs1057519813
GWAS Ctlgrs1057519813
Max Magnitude0
ClinVar
Risk rs1057519813(A;A)
Alt rs1057519813(A;A)
Reference Rs1057519813(G;G)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene PDGFRA
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000004.11:g.55152090G>A
CLNSRC
CLNACC RCV000443097.1,