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rs7779029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs7779029(C;C)
Make rs7779029(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position80902796
GeneSEMA3C
is asnp
is mentioned by
dbSNPrs7779029
dbSNP (classic)rs7779029
ClinGenrs7779029
ebirs7779029
HLIrs7779029
Exacrs7779029
Gnomadrs7779029
Varsomers7779029
LitVarrs7779029
Maprs7779029
PheGenIrs7779029
Biobankrs7779029
1000 genomesrs7779029
hgdprs7779029
ensemblrs7779029
geneviewrs7779029
scholarrs7779029
googlers7779029
pharmgkbrs7779029
gwascentralrs7779029
openSNPrs7779029
23andMers7779029
SNPshotrs7779029
SNPdbers7779029
MSV3drs7779029
GWAS Ctlgrs7779029
Max Magnitude0
? (C;C) (C;T) (T;T) 28


ClinVar
Risk rs7779029(C;C)
Alt rs7779029(C;C)
Reference Rs7779029(T;T)
Significance Drug-response
Disease irinotecan response - Toxicity/ADR
Variation info
Gene SEMA3C
CLNDBN irinotecan response - Toxicity/ADR
Reversed 0
HGVS NC_000007.13:g.80532112T>C
CLNSRC PharmGKB Clinical Annotation
CLNACC RCV000211136.1,