rs1057519707

Orientation

plus

Stabilized

plus

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

Make rs1057519707(A;G)

Make rs1057519707(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54728095

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057519707
dbSNP (classic)	rs1057519707
ClinGen	rs1057519707
ebi	rs1057519707
HLI	rs1057519707
Exac	rs1057519707
Gnomad	rs1057519707
Varsome	rs1057519707
LitVar	rs1057519707
Map	rs1057519707
PheGenI	rs1057519707
Biobank	rs1057519707
1000 genomes	rs1057519707
hgdp	rs1057519707
ensembl	rs1057519707
geneview	rs1057519707
scholar	rs1057519707
google	rs1057519707
pharmgkb	rs1057519707
gwascentral	rs1057519707
openSNP	rs1057519707
23andMe	rs1057519707
SNPshot	rs1057519707
SNPdbe	rs1057519707
MSV3d	rs1057519707
GWAS Ctlg	rs1057519707

Max Magnitude

0

ClinVar
Risk	rs1057519707(G;G)
Alt	rs1057519707(G;G)
Reference	Rs1057519707(A;A)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	KIT
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000004.11:g.55594261A>G
CLNSRC
CLNACC	RCV000438326.1,