rs121913520

Orientation

plus

Stabilized

plus

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

Make rs121913520(A;A)

Make rs121913520(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54727443

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs121913520
dbSNP (classic)	rs121913520
ClinGen	rs121913520
ebi	rs121913520
HLI	rs121913520
Exac	rs121913520
Gnomad	rs121913520
Varsome	rs121913520
LitVar	rs121913520
Map	rs121913520
PheGenI	rs121913520
Biobank	rs121913520
1000 genomes	rs121913520
hgdp	rs121913520
ensembl	rs121913520
geneview	rs121913520
scholar	rs121913520
google	rs121913520
pharmgkb	rs121913520
gwascentral	rs121913520
openSNP	rs121913520
23andMe	rs121913520
SNPshot	rs121913520
SNPdbe	rs121913520
MSV3d	rs121913520
GWAS Ctlg	rs121913520

Max Magnitude

0

ClinVar
Risk	rs121913520(A;A)
Alt	rs121913520(A;A)
Reference	Rs121913520(G;G)
Significance	Probable-Pathogenic
Disease	Myeloproliferative Neoplasm Gastrointestinal stromal tumor
Variation	info
Gene	KIT
CLNDBN	Myeloproliferative Neoplasm Gastrointestinal stromal tumor
Reversed	0
HGVS	NC_000004.11:g.55593609G>A
CLNSRC
CLNACC	RCV000426761.1, RCV000436995.1,