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rs1060500909

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060500909(C;C)
Make rs1060500909(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position103785717
GenePLP1, RAB9B
is asnp
is mentioned by
dbSNPrs1060500909
dbSNP (old)rs1060500909
ClinGenrs1060500909
ebirs1060500909
HLIrs1060500909
Exacrs1060500909
Gnomadrs1060500909
Varsomers1060500909
LitVarrs1060500909
Maprs1060500909
PheGenIrs1060500909
Biobankrs1060500909
1000 genomesrs1060500909
hgdprs1060500909
ensemblrs1060500909
gopubmedrs1060500909
geneviewrs1060500909
scholarrs1060500909
googlers1060500909
pharmgkbrs1060500909
gwascentralrs1060500909
openSNPrs1060500909
23andMers1060500909
23andMe allrs1060500909
SNPshotrs1060500909
SNPdbers1060500909
MSV3drs1060500909
GWAS Ctlgrs1060500909
Max Magnitude0
ClinVar
Risk rs1060500909(C;C)
Alt rs1060500909(C;C)
Reference Rs1060500909(T;T)
Significance Probable-Pathogenic
Disease Spastic paraplegia 2
Variation info
Gene PLP1 RAB9B
CLNDBN Spastic paraplegia 2
Reversed 0
HGVS NC_000023.10:g.103040646T>C
CLNSRC
CLNACC RCV000463096.1,