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rs587776803

From SNPedia

Orientationplus
Geno Mag Summary
(GTTGTT;GTTGTT) 0 common in clinvar
Make rs587776803(-;-)
Make rs587776803(-;TTGTTG)
Make rs587776803(TTGTTG;TTGTTG)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position54727444
GeneKIT
is asnp
is mentioned by
dbSNPrs587776803
ebirs587776803
HLIrs587776803
Exacrs587776803
Varsomers587776803
Maprs587776803
PheGenIrs587776803
hapmaprs587776803
1000 genomesrs587776803
hgdprs587776803
ensemblrs587776803
gopubmedrs587776803
geneviewrs587776803
scholarrs587776803
googlers587776803
pharmgkbrs587776803
gwascentralrs587776803
openSNPrs587776803
23andMers587776803
23andMe allrs587776803
SNP Nexus

SNPshotrs587776803
SNPdbers587776803
MSV3drs587776803
GWAS Ctlgrs587776803
Max Magnitude0
ClinVar
Risk rs587776803(;)
Alt rs587776803(;)
Reference rs587776803(GTTGTT;GTTGTT)
Significance Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene KIT
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55593610_55593615delTTGTTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000014858.4,