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rs148842275

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148842275(C;T)
Make rs148842275(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position80110767
GeneGAA
is asnp
is mentioned by
dbSNPrs148842275
dbSNP (old)rs148842275
ClinGenrs148842275
ebirs148842275
HLIrs148842275
Exacrs148842275
Gnomadrs148842275
Varsomers148842275
Maprs148842275
PheGenIrs148842275
Biobankrs148842275
1000 genomesrs148842275
hgdprs148842275
ensemblrs148842275
gopubmedrs148842275
geneviewrs148842275
scholarrs148842275
googlers148842275
pharmgkbrs148842275
gwascentralrs148842275
openSNPrs148842275
23andMers148842275
23andMe allrs148842275
SNPshotrs148842275
SNPdbers148842275
MSV3drs148842275
GWAS Ctlgrs148842275
Max Magnitude0
ClinVar
Risk rs148842275(T;T)
Alt rs148842275(T;T)
Reference Rs148842275(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GAA
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.78084566C>T
CLNSRC
CLNACC RCV000443985.1,