rs1057519706

Orientation

plus

Stabilized

plus

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

Make rs1057519706(G;G)

Make rs1057519706(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54727474

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057519706
dbSNP (classic)	rs1057519706
ClinGen	rs1057519706
ebi	rs1057519706
HLI	rs1057519706
Exac	rs1057519706
Gnomad	rs1057519706
Varsome	rs1057519706
LitVar	rs1057519706
Map	rs1057519706
PheGenI	rs1057519706
Biobank	rs1057519706
1000 genomes	rs1057519706
hgdp	rs1057519706
ensembl	rs1057519706
geneview	rs1057519706
scholar	rs1057519706
google	rs1057519706
pharmgkb	rs1057519706
gwascentral	rs1057519706
openSNP	rs1057519706
23andMe	rs1057519706
SNPshot	rs1057519706
SNPdbe	rs1057519706
MSV3d	rs1057519706
GWAS Ctlg	rs1057519706

Max Magnitude

0

ClinVar
Risk	rs1057519706(G;G)
Alt	rs1057519706(G;G)
Reference	Rs1057519706(T;T)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	KIT
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000004.11:g.55593640T>G
CLNSRC
CLNACC	RCV000442809.1,