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rs1057520032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520032(C;C)
Make rs1057520032(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54727438
GeneKIT
is asnp
is mentioned by
dbSNPrs1057520032
dbSNP (old)rs1057520032
ClinGenrs1057520032
ebirs1057520032
HLIrs1057520032
Exacrs1057520032
Gnomadrs1057520032
Varsomers1057520032
Maprs1057520032
PheGenIrs1057520032
Biobankrs1057520032
1000 genomesrs1057520032
hgdprs1057520032
ensemblrs1057520032
gopubmedrs1057520032
geneviewrs1057520032
scholarrs1057520032
googlers1057520032
pharmgkbrs1057520032
gwascentralrs1057520032
openSNPrs1057520032
23andMers1057520032
23andMe allrs1057520032
SNPshotrs1057520032
SNPdbers1057520032
MSV3drs1057520032
GWAS Ctlgrs1057520032
Max Magnitude0
ClinVar
Risk rs1057520032(C;C)
Alt rs1057520032(C;C)
Reference Rs1057520032(G;G)
Significance Probable-Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene KIT
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55593604G>C
CLNSRC
CLNACC RCV000438560.1,