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rs350099

From SNPedia

Orientationplus
Stabilizedplus
Make rs350099(C;C)
Make rs350099(C;T)
Make rs350099(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position69166129
GeneCCNB1
is asnp
is mentioned by
dbSNPrs350099
ebirs350099
HLIrs350099
Exacrs350099
Varsomers350099
Maprs350099
PheGenIrs350099
hapmaprs350099
1000 genomesrs350099
hgdprs350099
ensemblrs350099
gopubmedrs350099
geneviewrs350099
scholarrs350099
googlers350099
pharmgkbrs350099
gwascentralrs350099
openSNPrs350099
23andMers350099
23andMe allrs350099
SNP Nexus

SNPshotrs350099
SNPdbers350099
MSV3drs350099
GWAS Ctlgrs350099
Max Magnitude

[PMID 24395923] Genetic variants in CCNB1 associated with differential gene transcription and risk of coronary in-stent restenosis