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rs72653792

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72653792(G;T)
Make rs72653792(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position16178854
GeneABCC6
is asnp
is mentioned by
dbSNPrs72653792
dbSNP (classic)rs72653792
ClinGenrs72653792
ebirs72653792
HLIrs72653792
Exacrs72653792
Gnomadrs72653792
Varsomers72653792
LitVarrs72653792
Maprs72653792
PheGenIrs72653792
Biobankrs72653792
1000 genomesrs72653792
hgdprs72653792
ensemblrs72653792
geneviewrs72653792
scholarrs72653792
googlers72653792
pharmgkbrs72653792
gwascentralrs72653792
openSNPrs72653792
23andMers72653792
SNPshotrs72653792
SNPdbers72653792
MSV3drs72653792
GWAS Ctlgrs72653792
Max Magnitude0
ClinVar
Risk rs72653792(A;A) rs72653792(T;T)
Alt rs72653792(A;A) rs72653792(T;T)
Reference Rs72653792(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ABCC6
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.16272711C>T
CLNSRC
CLNACC RCV000483030.1,