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rs878855013

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855013(-;-)
Make rs878855013(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position67769731
GeneZFYVE26
is asnp
is mentioned by
dbSNPrs878855013
ebirs878855013
HLIrs878855013
Exacrs878855013
Varsomers878855013
Maprs878855013
PheGenIrs878855013
hapmaprs878855013
1000 genomesrs878855013
hgdprs878855013
ensemblrs878855013
gopubmedrs878855013
geneviewrs878855013
scholarrs878855013
googlers878855013
pharmgkbrs878855013
gwascentralrs878855013
openSNPrs878855013
23andMers878855013
23andMe allrs878855013
SNP Nexus

SNPshotrs878855013
SNPdbers878855013
MSV3drs878855013
GWAS Ctlgrs878855013
Max Magnitude0
ClinVar
Risk rs878855013(;)
Alt rs878855013(;)
Reference rs878855013(G;G)
Significance Probable-Pathogenic
Disease Spastic paraplegia
Variation info
Gene ZFYVE26
CLNDBN Spastic paraplegia
Reversed 1
HGVS NC_000014.8:g.68236448delC
CLNSRC
CLNACC RCV000227299.1,