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rs1060503426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1060503426(-;-)
Make rs1060503426(-;TC)
Make rs1060503426(TC;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89548078
GeneSPG7
is asnp
is mentioned by
dbSNPrs1060503426
dbSNP (old)rs1060503426
ClinGenrs1060503426
ebirs1060503426
HLIrs1060503426
Exacrs1060503426
Gnomadrs1060503426
Varsomers1060503426
LitVarrs1060503426
Maprs1060503426
PheGenIrs1060503426
Biobankrs1060503426
1000 genomesrs1060503426
hgdprs1060503426
ensemblrs1060503426
gopubmedrs1060503426
geneviewrs1060503426
scholarrs1060503426
googlers1060503426
pharmgkbrs1060503426
gwascentralrs1060503426
openSNPrs1060503426
23andMers1060503426
23andMe allrs1060503426
SNPshotrs1060503426
SNPdbers1060503426
MSV3drs1060503426
GWAS Ctlgrs1060503426
Max Magnitude0
ClinVar
Risk rs1060503426(-;-)
Alt rs1060503426(-;-)
Reference Rs1060503426(CT;CT)
Significance Pathogenic
Disease Spastic paraplegia 7
Variation info
Gene SPG7
CLNDBN Spastic paraplegia 7
Reversed 0
HGVS NC_000016.9:g.89614486_89614487delTC
CLNSRC
CLNACC RCV000472422.1,