rs1057519705

Orientation

plus

Stabilized

plus

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

Make rs1057519705(A;G)

Make rs1057519705(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54727464

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057519705
dbSNP (classic)	rs1057519705
ClinGen	rs1057519705
ebi	rs1057519705
HLI	rs1057519705
Exac	rs1057519705
Gnomad	rs1057519705
Varsome	rs1057519705
LitVar	rs1057519705
Map	rs1057519705
PheGenI	rs1057519705
Biobank	rs1057519705
1000 genomes	rs1057519705
hgdp	rs1057519705
ensembl	rs1057519705
geneview	rs1057519705
scholar	rs1057519705
google	rs1057519705
pharmgkb	rs1057519705
gwascentral	rs1057519705
openSNP	rs1057519705
23andMe	rs1057519705
SNPshot	rs1057519705
SNPdbe	rs1057519705
MSV3d	rs1057519705
GWAS Ctlg	rs1057519705

Max Magnitude

0

ClinVar
Risk	rs1057519705(G;G)
Alt	rs1057519705(G;G)
Reference	Rs1057519705(A;A)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	KIT
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000004.11:g.55593630A>G
CLNSRC
CLNACC	RCV000432830.1,