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rs879255241

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879255241(C;T)
Make rs879255241(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position57631225
GeneB4GALNT1
is asnp
is mentioned by
dbSNPrs879255241
ebirs879255241
HLIrs879255241
Exacrs879255241
Varsomers879255241
Maprs879255241
PheGenIrs879255241
hapmaprs879255241
1000 genomesrs879255241
hgdprs879255241
ensemblrs879255241
gopubmedrs879255241
geneviewrs879255241
scholarrs879255241
googlers879255241
pharmgkbrs879255241
gwascentralrs879255241
openSNPrs879255241
23andMers879255241
23andMe allrs879255241
SNP Nexus

SNPshotrs879255241
SNPdbers879255241
MSV3drs879255241
GWAS Ctlgrs879255241
Max Magnitude0
ClinVar
Risk rs879255241(T;T)
Alt rs879255241(T;T)
Reference rs879255241(C;C)
Significance Pathogenic
Disease Spastic paraplegia 26
Variation info
Gene B4GALNT1
CLNDBN Spastic paraplegia 26
Reversed 1
HGVS NC_000012.11:g.58025008G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000054422.2,