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rs786205474

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205474(A;A)
Make rs786205474(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position8605473
GeneAICDA
is asnp
is mentioned by
dbSNPrs786205474
ebirs786205474
HLIrs786205474
Exacrs786205474
Varsomers786205474
Maprs786205474
PheGenIrs786205474
hapmaprs786205474
1000 genomesrs786205474
hgdprs786205474
ensemblrs786205474
gopubmedrs786205474
geneviewrs786205474
scholarrs786205474
googlers786205474
pharmgkbrs786205474
gwascentralrs786205474
openSNPrs786205474
23andMers786205474
23andMe allrs786205474
SNP Nexus

SNPshotrs786205474
SNPdbers786205474
MSV3drs786205474
GWAS Ctlgrs786205474
Max Magnitude0
ClinVar
Risk rs786205474(A;A)
Alt rs786205474(A;A)
Reference rs786205474(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AICDA
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.8758069C>T
CLNSRC
CLNACC RCV000171206.1,