rs121913523

Orientation

plus

Stabilized

plus

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

Make rs121913523(C;C)

Make rs121913523(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54728092

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs121913523
dbSNP (classic)	rs121913523
ClinGen	rs121913523
ebi	rs121913523
HLI	rs121913523
Exac	rs121913523
Gnomad	rs121913523
Varsome	rs121913523
LitVar	rs121913523
Map	rs121913523
PheGenI	rs121913523
Biobank	rs121913523
1000 genomes	rs121913523
hgdp	rs121913523
ensembl	rs121913523
geneview	rs121913523
scholar	rs121913523
google	rs121913523
pharmgkb	rs121913523
gwascentral	rs121913523
openSNP	rs121913523
23andMe	rs121913523
SNPshot	rs121913523
SNPdbe	rs121913523
MSV3d	rs121913523
GWAS Ctlg	rs121913523

Max Magnitude

0

ClinVar
Risk	rs121913523(A;A) rs121913523(C;C)
Alt	rs121913523(A;A) rs121913523(C;C)
Reference	Rs121913523(T;T)
Significance	Pathogenic
Disease	Malignant melanoma Gastrointestinal stromal tumor
Variation	info
Gene	KIT
CLNDBN	Malignant melanoma Gastrointestinal stromal tumor
Reversed	0
HGVS	NC_000004.11:g.55594258T>A; NC_000004.11:g.55594258T>C
CLNSRC
CLNACC	RCV000439135.1, RCV000427620.1, RCV000442533.1,