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rs1057524664

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524664(G;T)
Make rs1057524664(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position80117094
GeneGAA
is asnp
is mentioned by
dbSNPrs1057524664
dbSNP (old)rs1057524664
ClinGenrs1057524664
ebirs1057524664
HLIrs1057524664
Exacrs1057524664
Gnomadrs1057524664
Varsomers1057524664
Maprs1057524664
PheGenIrs1057524664
Biobankrs1057524664
1000 genomesrs1057524664
hgdprs1057524664
ensemblrs1057524664
gopubmedrs1057524664
geneviewrs1057524664
scholarrs1057524664
googlers1057524664
pharmgkbrs1057524664
gwascentralrs1057524664
openSNPrs1057524664
23andMers1057524664
23andMe allrs1057524664
SNPshotrs1057524664
SNPdbers1057524664
MSV3drs1057524664
GWAS Ctlgrs1057524664
Max Magnitude0
ClinVar
Risk rs1057524664(T;T)
Alt rs1057524664(T;T)
Reference Rs1057524664(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GAA
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.78090893G>T
CLNSRC
CLNACC RCV000439307.1,