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rs1057519702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519702(C;C)
Make rs1057519702(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54726020
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519702
dbSNP (old)rs1057519702
ClinGenrs1057519702
ebirs1057519702
HLIrs1057519702
Exacrs1057519702
Gnomadrs1057519702
Varsomers1057519702
Maprs1057519702
PheGenIrs1057519702
Biobankrs1057519702
1000 genomesrs1057519702
hgdprs1057519702
ensemblrs1057519702
gopubmedrs1057519702
geneviewrs1057519702
scholarrs1057519702
googlers1057519702
pharmgkbrs1057519702
gwascentralrs1057519702
openSNPrs1057519702
23andMers1057519702
23andMe allrs1057519702
SNPshotrs1057519702
SNPdbers1057519702
MSV3drs1057519702
GWAS Ctlgrs1057519702
Max Magnitude0
ClinVar
Risk rs1057519702(C;C)
Alt rs1057519702(C;C)
Reference Rs1057519702(T;T)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene KIT
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000004.11:g.55592186T>C
CLNSRC
CLNACC RCV000430398.1,