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rs1057519811

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519811(C;T)
Make rs1057519811(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54274916
GenePDGFRA
is asnp
is mentioned by
dbSNPrs1057519811
dbSNP (old)rs1057519811
ClinGenrs1057519811
ebirs1057519811
HLIrs1057519811
Exacrs1057519811
Gnomadrs1057519811
Varsomers1057519811
Maprs1057519811
PheGenIrs1057519811
Biobankrs1057519811
1000 genomesrs1057519811
hgdprs1057519811
ensemblrs1057519811
gopubmedrs1057519811
geneviewrs1057519811
scholarrs1057519811
googlers1057519811
pharmgkbrs1057519811
gwascentralrs1057519811
openSNPrs1057519811
23andMers1057519811
23andMe allrs1057519811
SNPshotrs1057519811
SNPdbers1057519811
MSV3drs1057519811
GWAS Ctlgrs1057519811
Max Magnitude0
ClinVar
Risk rs1057519811(T;T)
Alt rs1057519811(T;T)
Reference Rs1057519811(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene PDGFRA
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000004.11:g.55141083C>T
CLNSRC
CLNACC RCV000423704.1,