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rs144016984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs144016984(A;G)
Make rs144016984(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position80117075
GeneGAA
is asnp
is mentioned by
dbSNPrs144016984
dbSNP (old)rs144016984
ClinGenrs144016984
ebirs144016984
HLIrs144016984
Exacrs144016984
Gnomadrs144016984
Varsomers144016984
Maprs144016984
PheGenIrs144016984
Biobankrs144016984
1000 genomesrs144016984
hgdprs144016984
ensemblrs144016984
gopubmedrs144016984
geneviewrs144016984
scholarrs144016984
googlers144016984
pharmgkbrs144016984
gwascentralrs144016984
openSNPrs144016984
23andMers144016984
23andMe allrs144016984
SNPshotrs144016984
SNPdbers144016984
MSV3drs144016984
GWAS Ctlgrs144016984
Max Magnitude0
ClinVar
Risk rs144016984(C;C) rs144016984(G;G)
Alt rs144016984(C;C) rs144016984(G;G)
Reference Rs144016984(A;A)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene GAA
CLNDBN not provided not specified
Reversed 0
HGVS NC_000017.10:g.78090874A>C; NC_000017.10:g.78090874A>G
CLNSRC
CLNACC RCV000486923.1, RCV000403113.1,