Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057520049

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520049(G;T)
Make rs1057520049(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position77360639
GeneVPS13A
is asnp
is mentioned by
dbSNPrs1057520049
dbSNP (old)rs1057520049
ClinGenrs1057520049
ebirs1057520049
HLIrs1057520049
Exacrs1057520049
Gnomadrs1057520049
Varsomers1057520049
Maprs1057520049
PheGenIrs1057520049
Biobankrs1057520049
1000 genomesrs1057520049
hgdprs1057520049
ensemblrs1057520049
gopubmedrs1057520049
geneviewrs1057520049
scholarrs1057520049
googlers1057520049
pharmgkbrs1057520049
gwascentralrs1057520049
openSNPrs1057520049
23andMers1057520049
23andMe allrs1057520049
SNPshotrs1057520049
SNPdbers1057520049
MSV3drs1057520049
GWAS Ctlgrs1057520049
Max Magnitude0
ClinVar
Risk rs1057520049(T;T)
Alt rs1057520049(T;T)
Reference Rs1057520049(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene VPS13A
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.79975555G>T
CLNSRC
CLNACC RCV000440207.1,