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rs1057519761

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519761(G;G)
Make rs1057519761(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position54733175
GeneKIT
is asnp
is mentioned by
dbSNPrs1057519761
dbSNP (old)rs1057519761
ClinGenrs1057519761
ebirs1057519761
HLIrs1057519761
Exacrs1057519761
Gnomadrs1057519761
Varsomers1057519761
Maprs1057519761
PheGenIrs1057519761
Biobankrs1057519761
1000 genomesrs1057519761
hgdprs1057519761
ensemblrs1057519761
gopubmedrs1057519761
geneviewrs1057519761
scholarrs1057519761
googlers1057519761
pharmgkbrs1057519761
gwascentralrs1057519761
openSNPrs1057519761
23andMers1057519761
23andMe allrs1057519761
SNPshotrs1057519761
SNPdbers1057519761
MSV3drs1057519761
GWAS Ctlgrs1057519761
Max Magnitude0
ClinVar
Risk rs1057519761(G;G)
Alt rs1057519761(G;G)
Reference Rs1057519761(T;T)
Significance Probable-Pathogenic
Disease Gastrointestinal stromal tumor
Variation info
Gene KIT
CLNDBN Gastrointestinal stromal tumor
Reversed 0
HGVS NC_000004.11:g.55599341T>G
CLNSRC
CLNACC RCV000439224.1,