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rs121913505

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913505(A;A)
Make rs121913505(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54695598
GeneKIT
is asnp
is mentioned by
dbSNPrs121913505
dbSNP (old)rs121913505
ClinGenrs121913505
ebirs121913505
HLIrs121913505
Exacrs121913505
Gnomadrs121913505
Varsomers121913505
Maprs121913505
PheGenIrs121913505
Biobankrs121913505
1000 genomesrs121913505
hgdprs121913505
ensemblrs121913505
gopubmedrs121913505
geneviewrs121913505
scholarrs121913505
googlers121913505
pharmgkbrs121913505
gwascentralrs121913505
openSNPrs121913505
23andMers121913505
23andMe allrs121913505
SNPshotrs121913505
SNPdbers121913505
MSV3drs121913505
GWAS Ctlgrs121913505
Max Magnitude0
ClinVar
Risk rs121913505(A;A)
Alt rs121913505(A;A)
Reference Rs121913505(G;G)
Significance Probable-Pathogenic
Disease Neoplasm Gastrointestinal stromal tumor
Variation info
Gene KIT
CLNDBN Neoplasm Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55561764G>A
CLNSRC
CLNACC RCV000422536.1, RCV000456243.1,