rs121913505

Orientation

plus

Stabilized

plus

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

Make rs121913505(A;A)

Make rs121913505(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54695598

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs121913505
dbSNP (classic)	rs121913505
ClinGen	rs121913505
ebi	rs121913505
HLI	rs121913505
Exac	rs121913505
Gnomad	rs121913505
Varsome	rs121913505
LitVar	rs121913505
Map	rs121913505
PheGenI	rs121913505
Biobank	rs121913505
1000 genomes	rs121913505
hgdp	rs121913505
ensembl	rs121913505
geneview	rs121913505
scholar	rs121913505
google	rs121913505
pharmgkb	rs121913505
gwascentral	rs121913505
openSNP	rs121913505
23andMe	rs121913505
SNPshot	rs121913505
SNPdbe	rs121913505
MSV3d	rs121913505
GWAS Ctlg	rs121913505

Max Magnitude

0

ClinVar
Risk	rs121913505(A;A)
Alt	rs121913505(A;A)
Reference	Rs121913505(G;G)
Significance	Probable-Pathogenic
Disease	Neoplasm Gastrointestinal stromal tumor
Variation	info
Gene	KIT
CLNDBN	Neoplasm Gastrointestinal stromal tumor
Reversed	0
HGVS	NC_000004.11:g.55561764G>A
CLNSRC
CLNACC	RCV000422536.1, RCV000456243.1,