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rs1057519707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519707(A;G)
Make rs1057519707(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54728095
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519707
dbSNP (classic)rs1057519707
ClinGenrs1057519707
ebirs1057519707
HLIrs1057519707
Exacrs1057519707
Gnomadrs1057519707
Varsomers1057519707
LitVarrs1057519707
Maprs1057519707
PheGenIrs1057519707
Biobankrs1057519707
1000 genomesrs1057519707
hgdprs1057519707
ensemblrs1057519707
geneviewrs1057519707
scholarrs1057519707
googlers1057519707
pharmgkbrs1057519707
gwascentralrs1057519707
openSNPrs1057519707
23andMers1057519707
23andMe allrs1057519707
SNPshotrs1057519707
SNPdbers1057519707
MSV3drs1057519707
GWAS Ctlgrs1057519707
Max Magnitude0
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,