rs1057519702

Orientation

plus

Stabilized

plus

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

Make rs1057519702(C;C)

Make rs1057519702(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54726020

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057519702
dbSNP (classic)	rs1057519702
ClinGen	rs1057519702
ebi	rs1057519702
HLI	rs1057519702
Exac	rs1057519702
Gnomad	rs1057519702
Varsome	rs1057519702
LitVar	rs1057519702
Map	rs1057519702
PheGenI	rs1057519702
Biobank	rs1057519702
1000 genomes	rs1057519702
hgdp	rs1057519702
ensembl	rs1057519702
geneview	rs1057519702
scholar	rs1057519702
google	rs1057519702
pharmgkb	rs1057519702
gwascentral	rs1057519702
openSNP	rs1057519702
23andMe	rs1057519702
SNPshot	rs1057519702
SNPdbe	rs1057519702
MSV3d	rs1057519702
GWAS Ctlg	rs1057519702

Max Magnitude

0

ClinVar
Risk	rs1057519702(C;C)
Alt	rs1057519702(C;C)
Reference	Rs1057519702(T;T)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	KIT
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000004.11:g.55592186T>C
CLNSRC
CLNACC	RCV000430398.1,