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rs1057520033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520033(C;C)
Make rs1057520033(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54727439
GeneKIT
is asnp
is mentioned by
dbSNPrs1057520033
dbSNP (classic)rs1057520033
ClinGenrs1057520033
ebirs1057520033
HLIrs1057520033
Exacrs1057520033
Gnomadrs1057520033
Varsomers1057520033
LitVarrs1057520033
Maprs1057520033
PheGenIrs1057520033
Biobankrs1057520033
1000 genomesrs1057520033
hgdprs1057520033
ensemblrs1057520033
geneviewrs1057520033
scholarrs1057520033
googlers1057520033
pharmgkbrs1057520033
gwascentralrs1057520033
openSNPrs1057520033
23andMers1057520033
23andMe allrs1057520033
SNPshotrs1057520033
SNPdbers1057520033
MSV3drs1057520033
GWAS Ctlgrs1057520033
Max Magnitude0
ClinVar
Risk rs1057520033(C;C)
Alt rs1057520033(C;C)
Reference Rs1057520033(G;G)
Significance Probable-Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene KIT
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55593605G>C
CLNSRC
CLNACC RCV000439662.1,