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

rs145798311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145798311(A;A)
Make rs145798311(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position88842769
GeneGALNS
is asnp
is mentioned by
dbSNPrs145798311
dbSNP (old)rs145798311
ClinGenrs145798311
ebirs145798311
HLIrs145798311
Exacrs145798311
Gnomadrs145798311
Varsomers145798311
Maprs145798311
PheGenIrs145798311
Biobankrs145798311
1000 genomesrs145798311
hgdprs145798311
ensemblrs145798311
gopubmedrs145798311
geneviewrs145798311
scholarrs145798311
googlers145798311
pharmgkbrs145798311
gwascentralrs145798311
openSNPrs145798311
23andMers145798311
23andMe allrs145798311
SNPshotrs145798311
SNPdbers145798311
MSV3drs145798311
GWAS Ctlgrs145798311
Max Magnitude0
ClinVar
Risk rs145798311(A;A)
Alt rs145798311(A;A)
Reference Rs145798311(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GALNS
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.88909177G>A
CLNSRC
CLNACC RCV000420201.1,