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rs1057519703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519703(A;C)
Make rs1057519703(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54727418
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519703
dbSNP (old)rs1057519703
ClinGenrs1057519703
ebirs1057519703
HLIrs1057519703
Exacrs1057519703
Gnomadrs1057519703
Varsomers1057519703
LitVarrs1057519703
Maprs1057519703
PheGenIrs1057519703
Biobankrs1057519703
1000 genomesrs1057519703
hgdprs1057519703
ensemblrs1057519703
gopubmedrs1057519703
geneviewrs1057519703
scholarrs1057519703
googlers1057519703
pharmgkbrs1057519703
gwascentralrs1057519703
openSNPrs1057519703
23andMers1057519703
23andMe allrs1057519703
SNPshotrs1057519703
SNPdbers1057519703
MSV3drs1057519703
GWAS Ctlgrs1057519703
Max Magnitude0
ClinVar
Risk rs1057519703(C;C) rs1057519703(T;T)
Alt rs1057519703(C;C) rs1057519703(T;T)
Reference Rs1057519703(A;A)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene KIT
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000004.11:g.55593584A>C; NC_000004.11:g.55593584A>T
CLNSRC
CLNACC RCV000441099.1, RCV000423846.1,