rs1057519700

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1057519700(A;A)

Make rs1057519700(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54277981

Gene

PDGFRA

is a	snp
is	mentioned by
dbSNP	rs1057519700
dbSNP (classic)	rs1057519700
ClinGen	rs1057519700
ebi	rs1057519700
HLI	rs1057519700
Exac	rs1057519700
Gnomad	rs1057519700
Varsome	rs1057519700
LitVar	rs1057519700
Map	rs1057519700
PheGenI	rs1057519700
Biobank	rs1057519700
1000 genomes	rs1057519700
hgdp	rs1057519700
ensembl	rs1057519700
geneview	rs1057519700
scholar	rs1057519700
google	rs1057519700
pharmgkb	rs1057519700
gwascentral	rs1057519700
openSNP	rs1057519700
23andMe	rs1057519700
SNPshot	rs1057519700
SNPdbe	rs1057519700
MSV3d	rs1057519700
GWAS Ctlg	rs1057519700

Max Magnitude

0

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,