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rs1064795251

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position99868332
GeneVPS13B
is asnp
is mentioned by
dbSNPrs1064795251
dbSNP (old)rs1064795251
ClinGenrs1064795251
ebirs1064795251
HLIrs1064795251
Exacrs1064795251
Gnomadrs1064795251
Varsomers1064795251
Maprs1064795251
PheGenIrs1064795251
Biobankrs1064795251
1000 genomesrs1064795251
hgdprs1064795251
ensemblrs1064795251
gopubmedrs1064795251
geneviewrs1064795251
scholarrs1064795251
googlers1064795251
pharmgkbrs1064795251
gwascentralrs1064795251
openSNPrs1064795251
23andMers1064795251
23andMe allrs1064795251
SNPshotrs1064795251
SNPdbers1064795251
MSV3drs1064795251
GWAS Ctlgrs1064795251
Max Magnitude0
ClinVar
Risk rs1064795251(-;-)
Alt rs1064795251(-;-)
Reference Rs1064795251(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene VPS13B
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.100880560delG
CLNSRC
CLNACC RCV000485494.1,