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rs1057518546

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518546(A;G)
Make rs1057518546(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome4
Position177437521
GeneAGA
is asnp
is mentioned by
dbSNPrs1057518546
dbSNP (old)rs1057518546
ClinGenrs1057518546
ebirs1057518546
HLIrs1057518546
Exacrs1057518546
Gnomadrs1057518546
Varsomers1057518546
Maprs1057518546
PheGenIrs1057518546
Biobankrs1057518546
1000 genomesrs1057518546
hgdprs1057518546
ensemblrs1057518546
gopubmedrs1057518546
geneviewrs1057518546
scholarrs1057518546
googlers1057518546
pharmgkbrs1057518546
gwascentralrs1057518546
openSNPrs1057518546
23andMers1057518546
23andMe allrs1057518546
SNPshotrs1057518546
SNPdbers1057518546
MSV3drs1057518546
GWAS Ctlgrs1057518546
Max Magnitude0
ClinVar
Risk rs1057518546(G;G)
Alt rs1057518546(G;G)
Reference Rs1057518546(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AGA
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.178358675T>C
CLNSRC
CLNACC RCV000413169.1,