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rs3900115

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 0 common in complete genomics
Make rs3900115(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position201185954
GeneCASP10
is asnp
is mentioned by
dbSNPrs3900115
dbSNP (old)rs3900115
ClinGenrs3900115
ebirs3900115
HLIrs3900115
Exacrs3900115
Gnomadrs3900115
Varsomers3900115
Maprs3900115
PheGenIrs3900115
Biobankrs3900115
1000 genomesrs3900115
hgdprs3900115
ensemblrs3900115
gopubmedrs3900115
geneviewrs3900115
scholarrs3900115
googlers3900115
pharmgkbrs3900115
gwascentralrs3900115
openSNPrs3900115
23andMers3900115
23andMe allrs3900115
SNP Nexus

SNPshotrs3900115
SNPdbers3900115
MSV3drs3900115
GWAS Ctlgrs3900115
GMAF0.4027
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 22568453] Association of CASP3 polymorphism with hematologic toxicity in advanced NSCLC patients treated with platinum-based chemotherapy

[PMID 17071630] Genetic variants in caspase genes and susceptibility to non-Hodgkin lymphoma.

[PMID 18381704OA-icon.png] Caspase polymorphisms and genetic susceptibility to multiple myeloma.

[PMID 19938081OA-icon.png] Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.


[PMID 23212337] Role of CASP-10 gene polymorphisms in cancer susceptibility: a HuGE review and meta-analysis


ClinVar
Risk rs3900115(G;G)
Alt rs3900115(G;G)
Reference Rs3900115(A;A)
Significance Non-pathogenic
Disease Autoimmune lymphoproliferative syndrome not specified
Variation info
Gene CASP10
CLNDBN Autoimmune lymphoproliferative syndrome not specified
Reversed 0
HGVS NC_000002.11:g.202050677A>G
CLNSRC
CLNACC RCV000384413.1, RCV000454697.1,