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rs139469785

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs139469785(C;T)
Make rs139469785(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position12337349
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs139469785
ebirs139469785
HLIrs139469785
Exacrs139469785
Varsomers139469785
Maprs139469785
PheGenIrs139469785
hapmaprs139469785
1000 genomesrs139469785
hgdprs139469785
ensemblrs139469785
gopubmedrs139469785
geneviewrs139469785
scholarrs139469785
googlers139469785
pharmgkbrs139469785
gwascentralrs139469785
openSNPrs139469785
23andMers139469785
23andMe allrs139469785
SNP Nexus

SNPshotrs139469785
SNPdbers139469785
MSV3drs139469785
GWAS Ctlgrs139469785
Max Magnitude0
ClinVar
Risk rs139469785(T;T)
Alt rs139469785(T;T)
Reference rs139469785(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AFG3L2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.12337348C>T
CLNSRC
CLNACC RCV000195592.2,