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rs34028295

From SNPedia

Orientationplus
Make rs34028295(-;-)
Make rs34028295(-;G)
Make rs34028295(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position50120124
GeneCOX14
is asnp
is mentioned by
dbSNPrs34028295
ebirs34028295
HLIrs34028295
Exacrs34028295
Varsomers34028295
Maprs34028295
PheGenIrs34028295
hapmaprs34028295
1000 genomesrs34028295
hgdprs34028295
ensemblrs34028295
gopubmedrs34028295
geneviewrs34028295
scholarrs34028295
googlers34028295
pharmgkbrs34028295
gwascentralrs34028295
openSNPrs34028295
23andMers34028295
23andMe allrs34028295
SNP Nexus

SNPshotrs34028295
SNPdbers34028295
MSV3drs34028295
GWAS Ctlgrs34028295
Max Magnitude
ClinVar
Risk rs34028295(G;G)
Alt rs34028295(G;G)
Reference rs34028295(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COX14
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.50513907dupG
CLNSRC
CLNACC RCV000196387.1,