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rs786205605

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205605(A;A)
Make rs786205605(A;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position103788464
GeneLOC101928286, PLP1
is asnp
is mentioned by
dbSNPrs786205605
ebirs786205605
HLIrs786205605
Exacrs786205605
Varsomers786205605
Maprs786205605
PheGenIrs786205605
hapmaprs786205605
1000 genomesrs786205605
hgdprs786205605
ensemblrs786205605
gopubmedrs786205605
geneviewrs786205605
scholarrs786205605
googlers786205605
pharmgkbrs786205605
gwascentralrs786205605
openSNPrs786205605
23andMers786205605
23andMe allrs786205605
SNP Nexus

SNPshotrs786205605
SNPdbers786205605
MSV3drs786205605
GWAS Ctlgrs786205605
Max Magnitude0
ClinVar
Risk rs786205605(A;A)
Alt rs786205605(A;A)
Reference rs786205605(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PLP1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.103043393G>A
CLNSRC
CLNACC RCV000171442.1,