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rs398123466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123466(A;A)
Make rs398123466(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position103788497
GenePLP1
is asnp
is mentioned by
dbSNPrs398123466
ebirs398123466
HLIrs398123466
Exacrs398123466
Varsomers398123466
Maprs398123466
PheGenIrs398123466
hapmaprs398123466
1000 genomesrs398123466
hgdprs398123466
ensemblrs398123466
gopubmedrs398123466
geneviewrs398123466
scholarrs398123466
googlers398123466
pharmgkbrs398123466
gwascentralrs398123466
openSNPrs398123466
23andMers398123466
23andMe allrs398123466
SNP Nexus

SNPshotrs398123466
SNPdbers398123466
MSV3drs398123466
GWAS Ctlgrs398123466
Max Magnitude0
ClinVar
Risk rs398123466(A;A)
Alt rs398123466(A;A)
Reference rs398123466(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PLP1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.103043426G>A
CLNSRC HGMD
CLNACC RCV000079101.4,