Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519814

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519814(C;T)
Make rs1057519814(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54285934
GenePDGFRA
is asnp
is mentioned by
dbSNPrs1057519814
dbSNP (classic)rs1057519814
ClinGenrs1057519814
ebirs1057519814
HLIrs1057519814
Exacrs1057519814
Gnomadrs1057519814
Varsomers1057519814
LitVarrs1057519814
Maprs1057519814
PheGenIrs1057519814
Biobankrs1057519814
1000 genomesrs1057519814
hgdprs1057519814
ensemblrs1057519814
geneviewrs1057519814
scholarrs1057519814
googlers1057519814
pharmgkbrs1057519814
gwascentralrs1057519814
openSNPrs1057519814
23andMers1057519814
23andMe allrs1057519814
SNPshotrs1057519814
SNPdbers1057519814
MSV3drs1057519814
GWAS Ctlgrs1057519814
Max Magnitude0
ClinVar
Risk rs1057519814(T;T)
Alt rs1057519814(T;T)
Reference Rs1057519814(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene PDGFRA
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000004.11:g.55152101C>T
CLNSRC
CLNACC RCV000427776.1,