rs1057520035

Orientation

plus

Stabilized

plus

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

Make rs1057520035(GG;TT)

Make rs1057520035(TT;TT)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54727438

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057520035
dbSNP (classic)	rs1057520035
ClinGen	rs1057520035
ebi	rs1057520035
HLI	rs1057520035
Exac	rs1057520035
Gnomad	rs1057520035
Varsome	rs1057520035
LitVar	rs1057520035
Map	rs1057520035
PheGenI	rs1057520035
Biobank	rs1057520035
1000 genomes	rs1057520035
hgdp	rs1057520035
ensembl	rs1057520035
geneview	rs1057520035
scholar	rs1057520035
google	rs1057520035
pharmgkb	rs1057520035
gwascentral	rs1057520035
openSNP	rs1057520035
23andMe	rs1057520035
SNPshot	rs1057520035
SNPdbe	rs1057520035
MSV3d	rs1057520035
GWAS Ctlg	rs1057520035

Max Magnitude

0

ClinVar
Risk	rs1057520035(TT;TT)
Alt	rs1057520035(TT;TT)
Reference	Rs1057520035(GG;GG)
Significance	Probable-Pathogenic
Disease	Gastrointestinal stromal tumor
Variation	info
Gene	KIT
CLNDBN	Gastrointestinal stromal tumor
Reversed	0
HGVS	NC_000004.11:g.55593604_55593605delGGinsTT
CLNSRC
CLNACC	RCV000428828.1,