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rs878853076

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853076(C;T)
Make rs878853076(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position103786661
GeneLOC101928286, PLP1
is asnp
is mentioned by
dbSNPrs878853076
ebirs878853076
HLIrs878853076
Exacrs878853076
Varsomers878853076
Maprs878853076
PheGenIrs878853076
hapmaprs878853076
1000 genomesrs878853076
hgdprs878853076
ensemblrs878853076
gopubmedrs878853076
geneviewrs878853076
scholarrs878853076
googlers878853076
pharmgkbrs878853076
gwascentralrs878853076
openSNPrs878853076
23andMers878853076
23andMe allrs878853076
SNP Nexus

SNPshotrs878853076
SNPdbers878853076
MSV3drs878853076
GWAS Ctlgrs878853076
Max Magnitude0
ClinVar
Risk rs878853076(T;T)
Alt rs878853076(T;T)
Reference rs878853076(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PLP1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.103041590C>T
CLNSRC
CLNACC RCV000223963.1,