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rs7500834

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs7500834(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position16178813
GeneABCC6
is asnp
is mentioned by
dbSNPrs7500834
ebirs7500834
HLIrs7500834
Exacrs7500834
Varsomers7500834
Maprs7500834
PheGenIrs7500834
hapmaprs7500834
1000 genomesrs7500834
hgdprs7500834
ensemblrs7500834
gopubmedrs7500834
geneviewrs7500834
scholarrs7500834
googlers7500834
pharmgkbrs7500834
gwascentralrs7500834
openSNPrs7500834
23andMers7500834
23andMe allrs7500834
SNP Nexus

SNPshotrs7500834
SNPdbers7500834
MSV3drs7500834
GWAS Ctlgrs7500834
GMAF0.0202
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs7500834(C;C)
Alt rs7500834(C;C)
Reference rs7500834(T;T)
Significance Untested
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000016.9:g.16272670T>C
CLNSRC
CLNACC