rs1057520032

Orientation

plus

Stabilized

plus

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

Make rs1057520032(C;C)

Make rs1057520032(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54727438

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057520032
dbSNP (classic)	rs1057520032
ClinGen	rs1057520032
ebi	rs1057520032
HLI	rs1057520032
Exac	rs1057520032
Gnomad	rs1057520032
Varsome	rs1057520032
LitVar	rs1057520032
Map	rs1057520032
PheGenI	rs1057520032
Biobank	rs1057520032
1000 genomes	rs1057520032
hgdp	rs1057520032
ensembl	rs1057520032
geneview	rs1057520032
scholar	rs1057520032
google	rs1057520032
pharmgkb	rs1057520032
gwascentral	rs1057520032
openSNP	rs1057520032
23andMe	rs1057520032
SNPshot	rs1057520032
SNPdbe	rs1057520032
MSV3d	rs1057520032
GWAS Ctlg	rs1057520032

Max Magnitude

0

ClinVar
Risk	rs1057520032(C;C)
Alt	rs1057520032(C;C)
Reference	Rs1057520032(G;G)
Significance	Probable-Pathogenic
Disease	Gastrointestinal stromal tumor
Variation	info
Gene	KIT
CLNDBN	Gastrointestinal stromal tumor
Reversed	0
HGVS	NC_000004.11:g.55593604G>C
CLNSRC
CLNACC	RCV000438560.1,