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rs1057520035

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs1057520035(GG;TT)
Make rs1057520035(TT;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54727438
GeneKIT
is asnp
is mentioned by
dbSNPrs1057520035
dbSNP (old)rs1057520035
ClinGenrs1057520035
ebirs1057520035
HLIrs1057520035
Exacrs1057520035
Gnomadrs1057520035
Varsomers1057520035
Maprs1057520035
PheGenIrs1057520035
Biobankrs1057520035
1000 genomesrs1057520035
hgdprs1057520035
ensemblrs1057520035
gopubmedrs1057520035
geneviewrs1057520035
scholarrs1057520035
googlers1057520035
pharmgkbrs1057520035
gwascentralrs1057520035
openSNPrs1057520035
23andMers1057520035
23andMe allrs1057520035
SNPshotrs1057520035
SNPdbers1057520035
MSV3drs1057520035
GWAS Ctlgrs1057520035
Max Magnitude0
ClinVar
Risk rs1057520035(TT;TT)
Alt rs1057520035(TT;TT)
Reference Rs1057520035(GG;GG)
Significance Probable-Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene KIT
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55593604_55593605delGGinsTT
CLNSRC
CLNACC RCV000428828.1,