rs121913234

Orientation

plus

Stabilized

plus

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

Make rs121913234(-;-)

Make rs121913234(-;AAACCCATGTATGAAGTACAGTGGAAG)

Make rs121913234(AAACCCATGTATGAAGTACAGTGGAAG;AAACCCATGTATGAAGTACAGTGGAAG)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

54727416

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs121913234
dbSNP (classic)	rs121913234
ClinGen	rs121913234
ebi	rs121913234
HLI	rs121913234
Exac	rs121913234
Gnomad	rs121913234
Varsome	rs121913234
LitVar	rs121913234
Map	rs121913234
PheGenI	rs121913234
Biobank	rs121913234
1000 genomes	rs121913234
hgdp	rs121913234
ensembl	rs121913234
geneview	rs121913234
scholar	rs121913234
google	rs121913234
pharmgkb	rs121913234
gwascentral	rs121913234
openSNP	rs121913234
23andMe	rs121913234
SNPshot	rs121913234
SNPdbe	rs121913234
MSV3d	rs121913234
GWAS Ctlg	rs121913234

Max Magnitude

0

ClinVar
Risk	rs121913234(-;-)
Alt	rs121913234(-;-)
Reference	Rs121913234(AGAAACCCATGTATGAAGTACAGTGGA;AGAAACCCATGTATGAAGTACAGTGGA)
Significance	Pathogenic
Disease	Gastrointestinal stromal tumor
Variation	info
Gene	KIT
CLNDBN	Gastrointestinal stromal tumor
Reversed	0
HGVS	NC_000004.11:g.55593582_55593608del27
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014871.4,