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rs869025568

From SNPedia

Orientationplus
Geno Mag Summary
(AGTGGA;AGTGGA) 0 common in clinvar
Make rs869025568(-;-)
Make rs869025568(-;TGGAAG)
Make rs869025568(TGGAAG;TGGAAG)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position54727437
GeneKIT
is asnp
is mentioned by
dbSNPrs869025568
ebirs869025568
HLIrs869025568
Exacrs869025568
Varsomers869025568
Maprs869025568
PheGenIrs869025568
hapmaprs869025568
1000 genomesrs869025568
hgdprs869025568
ensemblrs869025568
gopubmedrs869025568
geneviewrs869025568
scholarrs869025568
googlers869025568
pharmgkbrs869025568
gwascentralrs869025568
openSNPrs869025568
23andMers869025568
23andMe allrs869025568
SNP Nexus

SNPshotrs869025568
SNPdbers869025568
MSV3drs869025568
GWAS Ctlgrs869025568
Max Magnitude0
ClinVar
Risk rs869025568(;)
Alt rs869025568(;)
Reference rs869025568(AGTGGA;AGTGGA)
Significance Probable-Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene KIT
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55593603_55593608delTGGAAG
CLNSRC
CLNACC RCV000208566.1,