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rs9924755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9924755(A;A)
Make rs9924755(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position16177552
GeneABCC6
is asnp
is mentioned by
dbSNPrs9924755
ebirs9924755
HLIrs9924755
Exacrs9924755
Varsomers9924755
Maprs9924755
PheGenIrs9924755
hapmaprs9924755
1000 genomesrs9924755
hgdprs9924755
ensemblrs9924755
gopubmedrs9924755
geneviewrs9924755
scholarrs9924755
googlers9924755
pharmgkbrs9924755
gwascentralrs9924755
openSNPrs9924755
23andMers9924755
23andMe allrs9924755
SNP Nexus

SNPshotrs9924755
SNPdbers9924755
MSV3drs9924755
GWAS Ctlgrs9924755
GMAF0.1598
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs9924755(A;A)
Alt rs9924755(A;A)
Reference rs9924755(G;G)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 0
HGVS NC_000016.9:g.16271409G>A
CLNSRC
CLNACC



[PMID 10835642] Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum.