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rs1057519097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519097(A;G)
Make rs1057519097(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position8606929
GeneAICDA
is asnp
is mentioned by
dbSNPrs1057519097
dbSNP (old)rs1057519097
ClinGenrs1057519097
ebirs1057519097
HLIrs1057519097
Exacrs1057519097
Gnomadrs1057519097
Varsomers1057519097
Maprs1057519097
PheGenIrs1057519097
Biobankrs1057519097
1000 genomesrs1057519097
hgdprs1057519097
ensemblrs1057519097
gopubmedrs1057519097
geneviewrs1057519097
scholarrs1057519097
googlers1057519097
pharmgkbrs1057519097
gwascentralrs1057519097
openSNPrs1057519097
23andMers1057519097
23andMe allrs1057519097
SNPshotrs1057519097
SNPdbers1057519097
MSV3drs1057519097
GWAS Ctlgrs1057519097
Max Magnitude0
ClinVar
Risk rs1057519097(G;G)
Alt rs1057519097(G;G)
Reference Rs1057519097(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AICDA
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.8759525T>C
CLNSRC
CLNACC RCV000415972.2,