rs1057519708

Orientation

plus

Stabilized

plus

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

Make rs1057519708(A;A)

Make rs1057519708(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54728096

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057519708
dbSNP (classic)	rs1057519708
ClinGen	rs1057519708
ebi	rs1057519708
HLI	rs1057519708
Exac	rs1057519708
Gnomad	rs1057519708
Varsome	rs1057519708
LitVar	rs1057519708
Map	rs1057519708
PheGenI	rs1057519708
Biobank	rs1057519708
1000 genomes	rs1057519708
hgdp	rs1057519708
ensembl	rs1057519708
geneview	rs1057519708
scholar	rs1057519708
google	rs1057519708
pharmgkb	rs1057519708
gwascentral	rs1057519708
openSNP	rs1057519708
23andMe	rs1057519708
SNPshot	rs1057519708
SNPdbe	rs1057519708
MSV3d	rs1057519708
GWAS Ctlg	rs1057519708

Max Magnitude

0

ClinVar
Risk	rs1057519708(A;A) rs1057519708(G;G)
Alt	rs1057519708(A;A) rs1057519708(G;G)
Reference	Rs1057519708(T;T)
Significance	Pathogenic
Disease	Malignant melanoma
Variation	info
Gene	KIT
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000004.11:g.55594262T>A; NC_000004.11:g.55594262T>G
CLNSRC
CLNACC	RCV000417636.1, RCV000428319.1,