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rs863223866

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223866(A;A)
Make rs863223866(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position75076544
GeneABCB7
is asnp
is mentioned by
dbSNPrs863223866
ebirs863223866
HLIrs863223866
Exacrs863223866
Varsomers863223866
Maprs863223866
PheGenIrs863223866
hapmaprs863223866
1000 genomesrs863223866
hgdprs863223866
ensemblrs863223866
gopubmedrs863223866
geneviewrs863223866
scholarrs863223866
googlers863223866
pharmgkbrs863223866
gwascentralrs863223866
openSNPrs863223866
23andMers863223866
23andMe allrs863223866
SNP Nexus

SNPshotrs863223866
SNPdbers863223866
MSV3drs863223866
GWAS Ctlgrs863223866
Max Magnitude0
ClinVar
Risk rs863223866(A;A)
Alt rs863223866(A;A)
Reference rs863223866(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCB7
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.74296379C>T
CLNSRC
CLNACC RCV000199106.1,