rs1057520033

Orientation

plus

Stabilized

plus

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

Make rs1057520033(C;C)

Make rs1057520033(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54727439

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057520033
dbSNP (classic)	rs1057520033
ClinGen	rs1057520033
ebi	rs1057520033
HLI	rs1057520033
Exac	rs1057520033
Gnomad	rs1057520033
Varsome	rs1057520033
LitVar	rs1057520033
Map	rs1057520033
PheGenI	rs1057520033
Biobank	rs1057520033
1000 genomes	rs1057520033
hgdp	rs1057520033
ensembl	rs1057520033
geneview	rs1057520033
scholar	rs1057520033
google	rs1057520033
pharmgkb	rs1057520033
gwascentral	rs1057520033
openSNP	rs1057520033
23andMe	rs1057520033
SNPshot	rs1057520033
SNPdbe	rs1057520033
MSV3d	rs1057520033
GWAS Ctlg	rs1057520033

Max Magnitude

0

ClinVar
Risk	rs1057520033(C;C)
Alt	rs1057520033(C;C)
Reference	Rs1057520033(G;G)
Significance	Probable-Pathogenic
Disease	Gastrointestinal stromal tumor
Variation	info
Gene	KIT
CLNDBN	Gastrointestinal stromal tumor
Reversed	0
HGVS	NC_000004.11:g.55593605G>C
CLNSRC
CLNACC	RCV000439662.1,