Have questions? Visit https://www.reddit.com/r/SNPedia

rs387906860

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906860(-;-)
Make rs387906860(-;C)
Make rs387906860(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position16219577
GeneABCC6
is asnp
is mentioned by
dbSNPrs387906860
ebirs387906860
HLIrs387906860
Exacrs387906860
Varsomers387906860
Maprs387906860
PheGenIrs387906860
hapmaprs387906860
1000 genomesrs387906860
hgdprs387906860
ensemblrs387906860
gopubmedrs387906860
geneviewrs387906860
scholarrs387906860
googlers387906860
pharmgkbrs387906860
gwascentralrs387906860
openSNPrs387906860
23andMers387906860
23andMe allrs387906860
SNP Nexus

SNPshotrs387906860
SNPdbers387906860
MSV3drs387906860
GWAS Ctlgrs387906860
Max Magnitude0
ClinVar
Risk rs387906860(C;C)
Alt rs387906860(C;C)
Reference rs387906860(;)
Significance Pathogenic
Disease Generalized arterial calcification of infancy 2
Variation info
Gene ABCC6
CLNDBN Generalized arterial calcification of infancy 2
Reversed 1
HGVS NC_000016.9:g.16313435dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000023281.3,