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rs199474666

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199474666(A;G)
Make rs199474666(G;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position3274
GeneDDX27
is asnp
is mentioned by
dbSNPrs199474666
ebirs199474666
HLIrs199474666
Exacrs199474666
Varsomers199474666
Maprs199474666
PheGenIrs199474666
hapmaprs199474666
1000 genomesrs199474666
hgdprs199474666
ensemblrs199474666
gopubmedrs199474666
geneviewrs199474666
scholarrs199474666
googlers199474666
pharmgkbrs199474666
gwascentralrs199474666
openSNPrs199474666
23andMers199474666
23andMe allrs199474666
SNP Nexus

SNPshotrs199474666
SNPdbers199474666
MSV3drs199474666
GWAS Ctlgrs199474666
Max Magnitude0
ClinVar
Risk rs199474666(G;G)
Alt rs199474666(G;G)
Reference rs199474666(A;A)
Significance Pathogenic
Disease Neuropsychiatric disorder and early-onset cataract
Variation info
Gene
CLNDBN Neuropsychiatric disorder and early-onset cataract
Reversed 0
HGVS NC_012920.1:m.3274A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010221.2,