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rs863223867

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223867(G;G)
Make rs863223867(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position75076527
GeneABCB7
is asnp
is mentioned by
dbSNPrs863223867
ebirs863223867
HLIrs863223867
Exacrs863223867
Varsomers863223867
Maprs863223867
PheGenIrs863223867
hapmaprs863223867
1000 genomesrs863223867
hgdprs863223867
ensemblrs863223867
gopubmedrs863223867
geneviewrs863223867
scholarrs863223867
googlers863223867
pharmgkbrs863223867
gwascentralrs863223867
openSNPrs863223867
23andMers863223867
23andMe allrs863223867
SNP Nexus

SNPshotrs863223867
SNPdbers863223867
MSV3drs863223867
GWAS Ctlgrs863223867
Max Magnitude0
ClinVar
Risk rs863223867(G;G)
Alt rs863223867(G;G)
Reference rs863223867(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCB7
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.74296362A>C
CLNSRC
CLNACC RCV000195532.1,