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rs142223793

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142223793(A;A)
Make rs142223793(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position16178820
GeneABCC6
is asnp
is mentioned by
dbSNPrs142223793
dbSNP (classic)rs142223793
ClinGenrs142223793
ebirs142223793
HLIrs142223793
Exacrs142223793
Gnomadrs142223793
Varsomers142223793
LitVarrs142223793
Maprs142223793
PheGenIrs142223793
Biobankrs142223793
1000 genomesrs142223793
hgdprs142223793
ensemblrs142223793
geneviewrs142223793
scholarrs142223793
googlers142223793
pharmgkbrs142223793
gwascentralrs142223793
openSNPrs142223793
23andMers142223793
SNPshotrs142223793
SNPdbers142223793
MSV3drs142223793
GWAS Ctlgrs142223793
Max Magnitude0
ClinVar
Risk rs142223793(A;A)
Alt rs142223793(A;A)
Reference Rs142223793(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCC6
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.16272677G>A
CLNSRC
CLNACC RCV000489677.1,