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rs1057519182

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519182(G;G)
Make rs1057519182(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position99121241
GeneVPS13B
is asnp
is mentioned by
dbSNPrs1057519182
dbSNP (old)rs1057519182
ClinGenrs1057519182
ebirs1057519182
HLIrs1057519182
Exacrs1057519182
Gnomadrs1057519182
Varsomers1057519182
Maprs1057519182
PheGenIrs1057519182
Biobankrs1057519182
1000 genomesrs1057519182
hgdprs1057519182
ensemblrs1057519182
gopubmedrs1057519182
geneviewrs1057519182
scholarrs1057519182
googlers1057519182
pharmgkbrs1057519182
gwascentralrs1057519182
openSNPrs1057519182
23andMers1057519182
23andMe allrs1057519182
SNPshotrs1057519182
SNPdbers1057519182
MSV3drs1057519182
GWAS Ctlgrs1057519182
Max Magnitude0
ClinVar
Risk rs1057519182(G;G)
Alt rs1057519182(G;G)
Reference Rs1057519182(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene VPS13B
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.100133469T>G
CLNSRC
CLNACC RCV000416267.2,