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rs1057520769

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520769(A;T)
Make rs1057520769(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position99854124
GeneVPS13B
is asnp
is mentioned by
dbSNPrs1057520769
dbSNP (classic)rs1057520769
ClinGenrs1057520769
ebirs1057520769
HLIrs1057520769
Exacrs1057520769
Gnomadrs1057520769
Varsomers1057520769
LitVarrs1057520769
Maprs1057520769
PheGenIrs1057520769
Biobankrs1057520769
1000 genomesrs1057520769
hgdprs1057520769
ensemblrs1057520769
geneviewrs1057520769
scholarrs1057520769
googlers1057520769
pharmgkbrs1057520769
gwascentralrs1057520769
openSNPrs1057520769
23andMers1057520769
23andMe allrs1057520769
SNPshotrs1057520769
SNPdbers1057520769
MSV3drs1057520769
GWAS Ctlgrs1057520769
Max Magnitude0
ClinVar
Risk rs1057520769(T;T)
Alt rs1057520769(T;T)
Reference Rs1057520769(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene VPS13B
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.100866352A>T
CLNSRC
CLNACC RCV000429941.1,