rs1057519710

Orientation

plus

Stabilized

plus

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

Make rs1057519710(C;C)

Make rs1057519710(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54733166

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057519710
dbSNP (classic)	rs1057519710
ClinGen	rs1057519710
ebi	rs1057519710
HLI	rs1057519710
Exac	rs1057519710
Gnomad	rs1057519710
Varsome	rs1057519710
LitVar	rs1057519710
Map	rs1057519710
PheGenI	rs1057519710
Biobank	rs1057519710
1000 genomes	rs1057519710
hgdp	rs1057519710
ensembl	rs1057519710
geneview	rs1057519710
scholar	rs1057519710
google	rs1057519710
pharmgkb	rs1057519710
gwascentral	rs1057519710
openSNP	rs1057519710
23andMe	rs1057519710
SNPshot	rs1057519710
SNPdbe	rs1057519710
MSV3d	rs1057519710
GWAS Ctlg	rs1057519710

Max Magnitude

0

ClinVar
Risk	rs1057519710(C;C) rs1057519710(T;T)
Alt	rs1057519710(C;C) rs1057519710(T;T)
Reference	Rs1057519710(G;G)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	KIT
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000004.11:g.55599332G>C; NC_000004.11:g.55599332G>T
CLNSRC
CLNACC	RCV000427793.1, RCV000437969.1,