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rs63750763

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750763(C;T)
Make rs63750763(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position16150604
GeneABCC6
is asnp
is mentioned by
dbSNPrs63750763
ebirs63750763
HLIrs63750763
Exacrs63750763
Varsomers63750763
Maprs63750763
PheGenIrs63750763
hapmaprs63750763
1000 genomesrs63750763
hgdprs63750763
ensemblrs63750763
gopubmedrs63750763
geneviewrs63750763
scholarrs63750763
googlers63750763
pharmgkbrs63750763
gwascentralrs63750763
openSNPrs63750763
23andMers63750763
23andMe allrs63750763
SNP Nexus

SNPshotrs63750763
SNPdbers63750763
MSV3drs63750763
GWAS Ctlgrs63750763
Max Magnitude0
ClinVar
Risk rs63750763(T;T)
Alt rs63750763(T;T)
Reference rs63750763(C;C)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 1
HGVS NC_000016.9:g.16244461G>A
CLNSRC
CLNACC



[PMID 12673275] ABCC6/MRP6 mutations: further insight into the molecular pathology of pseudoxanthoma elasticum.