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rs1057520542

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520542(C;T)
Make rs1057520542(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position8605308
GeneAICDA
is asnp
is mentioned by
dbSNPrs1057520542
dbSNP (classic)rs1057520542
ClinGenrs1057520542
ebirs1057520542
HLIrs1057520542
Exacrs1057520542
Gnomadrs1057520542
Varsomers1057520542
LitVarrs1057520542
Maprs1057520542
PheGenIrs1057520542
Biobankrs1057520542
1000 genomesrs1057520542
hgdprs1057520542
ensemblrs1057520542
geneviewrs1057520542
scholarrs1057520542
googlers1057520542
pharmgkbrs1057520542
gwascentralrs1057520542
openSNPrs1057520542
23andMers1057520542
23andMe allrs1057520542
SNPshotrs1057520542
SNPdbers1057520542
MSV3drs1057520542
GWAS Ctlgrs1057520542
Max Magnitude0
ClinVar
Risk rs1057520542(T;T)
Alt rs1057520542(T;T)
Reference Rs1057520542(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene AICDA
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.8757904G>A
CLNSRC
CLNACC RCV000432589.1,