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rs1057518042

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518042(C;C)
Make rs1057518042(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position75070495
GeneABCB7
is asnp
is mentioned by
dbSNPrs1057518042
dbSNP (old)rs1057518042
ClinGenrs1057518042
ebirs1057518042
HLIrs1057518042
Exacrs1057518042
Gnomadrs1057518042
Varsomers1057518042
LitVarrs1057518042
Maprs1057518042
PheGenIrs1057518042
Biobankrs1057518042
1000 genomesrs1057518042
hgdprs1057518042
ensemblrs1057518042
gopubmedrs1057518042
geneviewrs1057518042
scholarrs1057518042
googlers1057518042
pharmgkbrs1057518042
gwascentralrs1057518042
openSNPrs1057518042
23andMers1057518042
23andMe allrs1057518042
SNPshotrs1057518042
SNPdbers1057518042
MSV3drs1057518042
GWAS Ctlgrs1057518042
Max Magnitude0
ClinVar
Risk rs1057518042(C;C)
Alt rs1057518042(C;C)
Reference Rs1057518042(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCB7
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.74290330A>G
CLNSRC
CLNACC RCV000412721.1,