rs121913513

Orientation

plus

Stabilized

plus

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

Make rs121913513(C;C)

Make rs121913513(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54727495

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs121913513
dbSNP (classic)	rs121913513
ClinGen	rs121913513
ebi	rs121913513
HLI	rs121913513
Exac	rs121913513
Gnomad	rs121913513
Varsome	rs121913513
LitVar	rs121913513
Map	rs121913513
PheGenI	rs121913513
Biobank	rs121913513
1000 genomes	rs121913513
hgdp	rs121913513
ensembl	rs121913513
geneview	rs121913513
scholar	rs121913513
google	rs121913513
pharmgkb	rs121913513
gwascentral	rs121913513
openSNP	rs121913513
23andMe	rs121913513
SNPshot	rs121913513
SNPdbe	rs121913513
MSV3d	rs121913513
GWAS Ctlg	rs121913513

Max Magnitude

0

ClinVar
Risk	rs121913513(C;C)
Alt	rs121913513(C;C)
Reference	Rs121913513(T;T)
Significance	Pathogenic
Disease	Malignant melanoma Non-small cell lung cancer Gastrointestinal stromal tumor Thymoma
Variation	info
Gene	KIT
CLNDBN	Malignant melanoma Non-small cell lung cancer Gastrointestinal stromal tumor Thymoma
Reversed	0
HGVS	NC_000004.11:g.55593661T>C
CLNSRC
CLNACC	RCV000426330.1, RCV000426967.1, RCV000433543.1, RCV000443552.1,