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rs786205553

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205553(G;T)
Make rs786205553(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome20
Position58444159
GeneVAPB
is asnp
is mentioned by
dbSNPrs786205553
ebirs786205553
HLIrs786205553
Exacrs786205553
Varsomers786205553
Maprs786205553
PheGenIrs786205553
hapmaprs786205553
1000 genomesrs786205553
hgdprs786205553
ensemblrs786205553
gopubmedrs786205553
geneviewrs786205553
scholarrs786205553
googlers786205553
pharmgkbrs786205553
gwascentralrs786205553
openSNPrs786205553
23andMers786205553
23andMe allrs786205553
SNP Nexus

SNPshotrs786205553
SNPdbers786205553
MSV3drs786205553
GWAS Ctlgrs786205553
Max Magnitude0
ClinVar
Risk rs786205553(T;T)
Alt rs786205553(T;T)
Reference rs786205553(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene VAPB
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.57019215G>T
CLNSRC
CLNACC RCV000171347.1,