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rs398123467

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123467(C;C)
Make rs398123467(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position103789373
GenePLP1
is asnp
is mentioned by
dbSNPrs398123467
ebirs398123467
HLIrs398123467
Exacrs398123467
Varsomers398123467
Maprs398123467
PheGenIrs398123467
hapmaprs398123467
1000 genomesrs398123467
hgdprs398123467
ensemblrs398123467
gopubmedrs398123467
geneviewrs398123467
scholarrs398123467
googlers398123467
pharmgkbrs398123467
gwascentralrs398123467
openSNPrs398123467
23andMers398123467
23andMe allrs398123467
SNP Nexus

SNPshotrs398123467
SNPdbers398123467
MSV3drs398123467
GWAS Ctlgrs398123467
Max Magnitude0
ClinVar
Risk rs398123467(C;C)
Alt rs398123467(C;C)
Reference rs398123467(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PLP1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.103044302G>C
CLNSRC HGMD
CLNACC RCV000079102.4,