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rs121913520

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913520(A;A)
Make rs121913520(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54727443
GeneKIT
is asnp
is mentioned by
dbSNPrs121913520
dbSNP (old)rs121913520
ClinGenrs121913520
ebirs121913520
HLIrs121913520
Exacrs121913520
Gnomadrs121913520
Varsomers121913520
Maprs121913520
PheGenIrs121913520
Biobankrs121913520
1000 genomesrs121913520
hgdprs121913520
ensemblrs121913520
gopubmedrs121913520
geneviewrs121913520
scholarrs121913520
googlers121913520
pharmgkbrs121913520
gwascentralrs121913520
openSNPrs121913520
23andMers121913520
23andMe allrs121913520
SNPshotrs121913520
SNPdbers121913520
MSV3drs121913520
GWAS Ctlgrs121913520
Max Magnitude0
ClinVar
Risk rs121913520(A;A)
Alt rs121913520(A;A)
Reference Rs121913520(G;G)
Significance Probable-Pathogenic
Disease Myeloproliferative Neoplasm Gastrointestinal stromal tumor
Variation info
Gene KIT
CLNDBN Myeloproliferative Neoplasm Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55593609G>A
CLNSRC
CLNACC RCV000426761.1, RCV000436995.1,