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rs1057519700

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519700(A;A)
Make rs1057519700(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54277981
GenePDGFRA
is asnp
is mentioned by
dbSNPrs1057519700
dbSNP (old)rs1057519700
ClinGenrs1057519700
ebirs1057519700
HLIrs1057519700
Exacrs1057519700
Gnomadrs1057519700
Varsomers1057519700
LitVarrs1057519700
Maprs1057519700
PheGenIrs1057519700
Biobankrs1057519700
1000 genomesrs1057519700
hgdprs1057519700
ensemblrs1057519700
gopubmedrs1057519700
geneviewrs1057519700
scholarrs1057519700
googlers1057519700
pharmgkbrs1057519700
gwascentralrs1057519700
openSNPrs1057519700
23andMers1057519700
23andMe allrs1057519700
SNPshotrs1057519700
SNPdbers1057519700
MSV3drs1057519700
GWAS Ctlgrs1057519700
Max Magnitude0
ClinVar
Risk rs1057519700(A;A) rs1057519700(G;G)
Alt rs1057519700(A;A) rs1057519700(G;G)
Reference Rs1057519700(C;C)
Significance Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene PDGFRA
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55144148C>A; NC_000004.11:g.55144148C>G
CLNSRC
CLNACC RCV000419062.1, RCV000429785.1,