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rs63750018

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750018(C;C)
Make rs63750018(C;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position16154776
GeneABCC6
is asnp
is mentioned by
dbSNPrs63750018
ebirs63750018
HLIrs63750018
Exacrs63750018
Varsomers63750018
Maprs63750018
PheGenIrs63750018
hapmaprs63750018
1000 genomesrs63750018
hgdprs63750018
ensemblrs63750018
gopubmedrs63750018
geneviewrs63750018
scholarrs63750018
googlers63750018
pharmgkbrs63750018
gwascentralrs63750018
openSNPrs63750018
23andMers63750018
23andMe allrs63750018
SNP Nexus

SNPshotrs63750018
SNPdbers63750018
MSV3drs63750018
GWAS Ctlgrs63750018
Max Magnitude0
ClinVar
Risk rs63750018(C;C)
Alt rs63750018(C;C)
Reference rs63750018(G;G)
Significance Untested
Disease
Variation info
Gene ABCC6
CLNDBN
Reversed 1
HGVS NC_000016.9:g.16248633C>G
CLNSRC
CLNACC



[PMID 11702217] Identification of ABCC6 pseudogenes on human chromosome 16p: implications for mutation detection in pseudoxanthoma elasticum.