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rs1060502521

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502521(-;-)
Make rs1060502521(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54733162
GeneKIT
is asnp
is mentioned by
dbSNPrs1060502521
dbSNP (old)rs1060502521
ClinGenrs1060502521
ebirs1060502521
HLIrs1060502521
Exacrs1060502521
Gnomadrs1060502521
Varsomers1060502521
LitVarrs1060502521
Maprs1060502521
PheGenIrs1060502521
Biobankrs1060502521
1000 genomesrs1060502521
hgdprs1060502521
ensemblrs1060502521
gopubmedrs1060502521
geneviewrs1060502521
scholarrs1060502521
googlers1060502521
pharmgkbrs1060502521
gwascentralrs1060502521
openSNPrs1060502521
23andMers1060502521
23andMe allrs1060502521
SNPshotrs1060502521
SNPdbers1060502521
MSV3drs1060502521
GWAS Ctlgrs1060502521
Max Magnitude0
ClinVar
Risk rs1060502521(-;-)
Alt rs1060502521(-;-)
Reference Rs1060502521(G;G)
Significance Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene KIT
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55599328delG
CLNSRC
CLNACC RCV000470229.1,