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rs1057519704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519704(A;A)
Make rs1057519704(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54727425
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519704
dbSNP (classic)rs1057519704
ClinGenrs1057519704
ebirs1057519704
HLIrs1057519704
Exacrs1057519704
Gnomadrs1057519704
Varsomers1057519704
LitVarrs1057519704
Maprs1057519704
PheGenIrs1057519704
Biobankrs1057519704
1000 genomesrs1057519704
hgdprs1057519704
ensemblrs1057519704
geneviewrs1057519704
scholarrs1057519704
googlers1057519704
pharmgkbrs1057519704
gwascentralrs1057519704
openSNPrs1057519704
23andMers1057519704
SNPshotrs1057519704
SNPdbers1057519704
MSV3drs1057519704
GWAS Ctlgrs1057519704
Max Magnitude0
ClinVar
Risk rs1057519704(A;A)
Alt rs1057519704(A;A)
Reference Rs1057519704(T;T)
Significance Pathogenic
Disease Malignant melanoma Thymoma
Variation info
Gene KIT
CLNDBN Malignant melanoma Thymoma
Reversed 0
HGVS NC_000004.11:g.55593591T>A
CLNSRC
CLNACC RCV000434537.1, RCV000438425.1,