rs1057519761

Orientation

plus

Stabilized

plus

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

Make rs1057519761(G;G)

Make rs1057519761(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54733175

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057519761
dbSNP (classic)	rs1057519761
ClinGen	rs1057519761
ebi	rs1057519761
HLI	rs1057519761
Exac	rs1057519761
Gnomad	rs1057519761
Varsome	rs1057519761
LitVar	rs1057519761
Map	rs1057519761
PheGenI	rs1057519761
Biobank	rs1057519761
1000 genomes	rs1057519761
hgdp	rs1057519761
ensembl	rs1057519761
geneview	rs1057519761
scholar	rs1057519761
google	rs1057519761
pharmgkb	rs1057519761
gwascentral	rs1057519761
openSNP	rs1057519761
23andMe	rs1057519761
SNPshot	rs1057519761
SNPdbe	rs1057519761
MSV3d	rs1057519761
GWAS Ctlg	rs1057519761

Max Magnitude

0

ClinVar
Risk	rs1057519761(G;G)
Alt	rs1057519761(G;G)
Reference	Rs1057519761(T;T)
Significance	Probable-Pathogenic
Disease	Gastrointestinal stromal tumor
Variation	info
Gene	KIT
CLNDBN	Gastrointestinal stromal tumor
Reversed	0
HGVS	NC_000004.11:g.55599341T>G
CLNSRC
CLNACC	RCV000439224.1,