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rs1057519708

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519708(A;A)
Make rs1057519708(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54728096
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519708
dbSNP (old)rs1057519708
ClinGenrs1057519708
ebirs1057519708
HLIrs1057519708
Exacrs1057519708
Gnomadrs1057519708
Varsomers1057519708
Maprs1057519708
PheGenIrs1057519708
Biobankrs1057519708
1000 genomesrs1057519708
hgdprs1057519708
ensemblrs1057519708
gopubmedrs1057519708
geneviewrs1057519708
scholarrs1057519708
googlers1057519708
pharmgkbrs1057519708
gwascentralrs1057519708
openSNPrs1057519708
23andMers1057519708
23andMe allrs1057519708
SNPshotrs1057519708
SNPdbers1057519708
MSV3drs1057519708
GWAS Ctlgrs1057519708
Max Magnitude0
ClinVar
Risk rs1057519708(A;A) rs1057519708(G;G)
Alt rs1057519708(A;A) rs1057519708(G;G)
Reference Rs1057519708(T;T)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene KIT
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000004.11:g.55594262T>A; NC_000004.11:g.55594262T>G
CLNSRC
CLNACC RCV000417636.1, RCV000428319.1,