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rs1057518228

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518228(-;AGGG)
Make rs1057518228(AGGG;AGGG)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position99861905
GeneVPS13B
is asnp
is mentioned by
dbSNPrs1057518228
dbSNP (old)rs1057518228
ClinGenrs1057518228
ebirs1057518228
HLIrs1057518228
Exacrs1057518228
Gnomadrs1057518228
Varsomers1057518228
Maprs1057518228
PheGenIrs1057518228
Biobankrs1057518228
1000 genomesrs1057518228
hgdprs1057518228
ensemblrs1057518228
gopubmedrs1057518228
geneviewrs1057518228
scholarrs1057518228
googlers1057518228
pharmgkbrs1057518228
gwascentralrs1057518228
openSNPrs1057518228
23andMers1057518228
23andMe allrs1057518228
SNPshotrs1057518228
SNPdbers1057518228
MSV3drs1057518228
GWAS Ctlgrs1057518228
Max Magnitude0
ClinVar
Risk rs1057518228(GAGG;GAGG)
Alt rs1057518228(GAGG;GAGG)
Reference Rs1057518228(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene VPS13B
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.100874130_100874133dupAGGG
CLNSRC
CLNACC RCV000413268.1,