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rs72653759

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72653759(C;G)
Make rs72653759(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position16202086
GeneABCC6
is asnp
is mentioned by
dbSNPrs72653759
ebirs72653759
HLIrs72653759
Exacrs72653759
Varsomers72653759
Maprs72653759
PheGenIrs72653759
hapmaprs72653759
1000 genomesrs72653759
hgdprs72653759
ensemblrs72653759
gopubmedrs72653759
geneviewrs72653759
scholarrs72653759
googlers72653759
pharmgkbrs72653759
gwascentralrs72653759
openSNPrs72653759
23andMers72653759
23andMe allrs72653759
SNP Nexus

SNPshotrs72653759
SNPdbers72653759
MSV3drs72653759
GWAS Ctlgrs72653759
Max Magnitude0
ClinVar
Risk rs72653759(G;G)
Alt rs72653759(G;G)
Reference rs72653759(C;C)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 1
HGVS NC_000016.9:g.16295943G>C
CLNSRC
CLNACC



[PMID 11702217] Identification of ABCC6 pseudogenes on human chromosome 16p: implications for mutation detection in pseudoxanthoma elasticum.