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rs1060503427

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1060503427(-;T)
Make rs1060503427(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89553953
GeneSPG7
is asnp
is mentioned by
dbSNPrs1060503427
dbSNP (old)rs1060503427
ClinGenrs1060503427
ebirs1060503427
HLIrs1060503427
Exacrs1060503427
Gnomadrs1060503427
Varsomers1060503427
Maprs1060503427
PheGenIrs1060503427
Biobankrs1060503427
1000 genomesrs1060503427
hgdprs1060503427
ensemblrs1060503427
gopubmedrs1060503427
geneviewrs1060503427
scholarrs1060503427
googlers1060503427
pharmgkbrs1060503427
gwascentralrs1060503427
openSNPrs1060503427
23andMers1060503427
23andMe allrs1060503427
SNPshotrs1060503427
SNPdbers1060503427
MSV3drs1060503427
GWAS Ctlgrs1060503427
Max Magnitude0
ClinVar
Risk rs1060503427(T;T)
Alt rs1060503427(T;T)
Reference Rs1060503427(-;-)
Significance Pathogenic
Disease Spastic paraplegia 7 not provided
Variation info
Gene SPG7
CLNDBN Spastic paraplegia 7 not provided
Reversed 0
HGVS NC_000016.9:g.89620361dupT
CLNSRC
CLNACC RCV000460135.1, RCV000489898.1,