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rs200280742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200280742(C;T)
Make rs200280742(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position77302991
GeneVPS13A
is asnp
is mentioned by
dbSNPrs200280742
dbSNP (old)rs200280742
ClinGenrs200280742
ebirs200280742
HLIrs200280742
Exacrs200280742
Gnomadrs200280742
Varsomers200280742
Maprs200280742
PheGenIrs200280742
Biobankrs200280742
1000 genomesrs200280742
hgdprs200280742
ensemblrs200280742
gopubmedrs200280742
geneviewrs200280742
scholarrs200280742
googlers200280742
pharmgkbrs200280742
gwascentralrs200280742
openSNPrs200280742
23andMers200280742
23andMe allrs200280742
SNPshotrs200280742
SNPdbers200280742
MSV3drs200280742
GWAS Ctlgrs200280742
Max Magnitude0
ClinVar
Risk rs200280742(T;T)
Alt rs200280742(T;T)
Reference Rs200280742(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene VPS13A
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.79917907C>T
CLNSRC
CLNACC RCV000413108.1,