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rs1060503425

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs1060503425(AGC;AGC)
Make rs1060503425(AGC;GG)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89531961
GeneSPG7
is asnp
is mentioned by
dbSNPrs1060503425
dbSNP (old)rs1060503425
ClinGenrs1060503425
ebirs1060503425
HLIrs1060503425
Exacrs1060503425
Gnomadrs1060503425
Varsomers1060503425
Maprs1060503425
PheGenIrs1060503425
Biobankrs1060503425
1000 genomesrs1060503425
hgdprs1060503425
ensemblrs1060503425
gopubmedrs1060503425
geneviewrs1060503425
scholarrs1060503425
googlers1060503425
pharmgkbrs1060503425
gwascentralrs1060503425
openSNPrs1060503425
23andMers1060503425
23andMe allrs1060503425
SNPshotrs1060503425
SNPdbers1060503425
MSV3drs1060503425
GWAS Ctlgrs1060503425
Max Magnitude0
ClinVar
Risk rs1060503425(AGC;AGC)
Alt rs1060503425(AGC;AGC)
Reference Rs1060503425(GG;GG)
Significance Pathogenic
Disease Spastic paraplegia 7
Variation info
Gene SPG7
CLNDBN Spastic paraplegia 7
Reversed 0
HGVS NC_000016.9:g.89598369_89598370delGGinsAGC
CLNSRC
CLNACC RCV000465046.1,