Have questions? Visit https://www.reddit.com/r/SNPedia

rs1133577

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1133577(G;T)
Make rs1133577(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position75073944
GeneABCB7
is asnp
is mentioned by
dbSNPrs1133577
ebirs1133577
HLIrs1133577
Exacrs1133577
Varsomers1133577
Maprs1133577
PheGenIrs1133577
hapmaprs1133577
1000 genomesrs1133577
hgdprs1133577
ensemblrs1133577
gopubmedrs1133577
geneviewrs1133577
scholarrs1133577
googlers1133577
pharmgkbrs1133577
gwascentralrs1133577
openSNPrs1133577
23andMers1133577
23andMe allrs1133577
SNP Nexus

SNPshotrs1133577
SNPdbers1133577
MSV3drs1133577
GWAS Ctlgrs1133577
Max Magnitude0
ClinVar
Risk rs1133577(T;T)
Alt rs1133577(T;T)
Reference rs1133577(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCB7
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.74293779C>T
CLNSRC
CLNACC RCV000199533.2,