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rs1057519710

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519710(C;C)
Make rs1057519710(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54733166
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519710
dbSNP (classic)rs1057519710
ClinGenrs1057519710
ebirs1057519710
HLIrs1057519710
Exacrs1057519710
Gnomadrs1057519710
Varsomers1057519710
LitVarrs1057519710
Maprs1057519710
PheGenIrs1057519710
Biobankrs1057519710
1000 genomesrs1057519710
hgdprs1057519710
ensemblrs1057519710
geneviewrs1057519710
scholarrs1057519710
googlers1057519710
pharmgkbrs1057519710
gwascentralrs1057519710
openSNPrs1057519710
23andMers1057519710
23andMe allrs1057519710
SNPshotrs1057519710
SNPdbers1057519710
MSV3drs1057519710
GWAS Ctlgrs1057519710
Max Magnitude0
ClinVar
Risk rs1057519710(C;C) rs1057519710(T;T)
Alt rs1057519710(C;C) rs1057519710(T;T)
Reference Rs1057519710(G;G)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene KIT
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000004.11:g.55599332G>C; NC_000004.11:g.55599332G>T
CLNSRC
CLNACC RCV000427793.1, RCV000437969.1,