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rs59002125

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs59002125(C;T)
Make rs59002125(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position16182884
GeneABCC6
is asnp
is mentioned by
dbSNPrs59002125
ebirs59002125
HLIrs59002125
Exacrs59002125
Varsomers59002125
Maprs59002125
PheGenIrs59002125
hapmaprs59002125
1000 genomesrs59002125
hgdprs59002125
ensemblrs59002125
gopubmedrs59002125
geneviewrs59002125
scholarrs59002125
googlers59002125
pharmgkbrs59002125
gwascentralrs59002125
openSNPrs59002125
23andMers59002125
23andMe allrs59002125
SNP Nexus

SNPshotrs59002125
SNPdbers59002125
MSV3drs59002125
GWAS Ctlgrs59002125
GMAF0.001377
Max Magnitude0
ClinVar
Risk rs59002125(T;T)
Alt rs59002125(T;T)
Reference rs59002125(C;C)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 1
HGVS NC_000016.9:g.16276741G>A
CLNSRC
CLNACC



[PMID 16127278] Analysis of sequence variations in the ABCC6 gene among patients with abdominal aortic aneurysm and pseudoxanthoma elasticum.