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rs1057519706

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519706(G;G)
Make rs1057519706(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54727474
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519706
dbSNP (old)rs1057519706
ClinGenrs1057519706
ebirs1057519706
HLIrs1057519706
Exacrs1057519706
Gnomadrs1057519706
Varsomers1057519706
Maprs1057519706
PheGenIrs1057519706
Biobankrs1057519706
1000 genomesrs1057519706
hgdprs1057519706
ensemblrs1057519706
gopubmedrs1057519706
geneviewrs1057519706
scholarrs1057519706
googlers1057519706
pharmgkbrs1057519706
gwascentralrs1057519706
openSNPrs1057519706
23andMers1057519706
23andMe allrs1057519706
SNPshotrs1057519706
SNPdbers1057519706
MSV3drs1057519706
GWAS Ctlgrs1057519706
Max Magnitude0
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,