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rs1057519705

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519705(A;G)
Make rs1057519705(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54727464
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519705
dbSNP (old)rs1057519705
ClinGenrs1057519705
ebirs1057519705
HLIrs1057519705
Exacrs1057519705
Gnomadrs1057519705
Varsomers1057519705
Maprs1057519705
PheGenIrs1057519705
Biobankrs1057519705
1000 genomesrs1057519705
hgdprs1057519705
ensemblrs1057519705
gopubmedrs1057519705
geneviewrs1057519705
scholarrs1057519705
googlers1057519705
pharmgkbrs1057519705
gwascentralrs1057519705
openSNPrs1057519705
23andMers1057519705
23andMe allrs1057519705
SNPshotrs1057519705
SNPdbers1057519705
MSV3drs1057519705
GWAS Ctlgrs1057519705
Max Magnitude0
ClinVar
Risk rs1057519705(G;G)
Alt rs1057519705(G;G)
Reference Rs1057519705(A;A)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene KIT
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000004.11:g.55593630A>G
CLNSRC
CLNACC RCV000432830.1,