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rs121918358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918358(A;A)
Make rs121918358(A;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position89510539
GeneSPG7
is asnp
is mentioned by
dbSNPrs121918358
ebirs121918358
HLIrs121918358
Exacrs121918358
Varsomers121918358
Maprs121918358
PheGenIrs121918358
hapmaprs121918358
1000 genomesrs121918358
hgdprs121918358
ensemblrs121918358
gopubmedrs121918358
geneviewrs121918358
scholarrs121918358
googlers121918358
pharmgkbrs121918358
gwascentralrs121918358
openSNPrs121918358
23andMers121918358
23andMe allrs121918358
SNP Nexus

SNPshotrs121918358
SNPdbers121918358
MSV3drs121918358
GWAS Ctlgrs121918358
Max Magnitude0
OMIM602783
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918358(A;A)
Alt rs121918358(A;A)
Reference rs121918358(T;T)
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.89576947T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007218.5, RCV000200640.2,