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rs17084733

From SNPedia

Orientationplus
Make rs17084733(A;A)
Make rs17084733(A;G)
Make rs17084733(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome4
Position54738774
GeneKIT
is asnp
is mentioned by
dbSNPrs17084733
dbSNP (classic)rs17084733
ClinGenrs17084733
ebirs17084733
HLIrs17084733
Exacrs17084733
Gnomadrs17084733
Varsomers17084733
LitVarrs17084733
Maprs17084733
PheGenIrs17084733
Biobankrs17084733
1000 genomesrs17084733
hgdprs17084733
ensemblrs17084733
geneviewrs17084733
scholarrs17084733
googlers17084733
pharmgkbrs17084733
gwascentralrs17084733
openSNPrs17084733
23andMers17084733
SNPshotrs17084733
SNPdbers17084733
MSV3drs17084733
GWAS Ctlgrs17084733
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 30983504OA-icon.png] The rs17084733 variant in the KIT 3' UTR disrupts a miR-221/222 binding site in gastrointestinal stromal tumour: a sponge-like mechanism conferring disease susceptibility.