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rs779805236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs779805236(A;G)
Make rs779805236(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position12370847
GeneAFG3L2
is asnp
is mentioned by
dbSNPrs779805236
dbSNP (classic)rs779805236
ClinGenrs779805236
ebirs779805236
HLIrs779805236
Exacrs779805236
Gnomadrs779805236
Varsomers779805236
LitVarrs779805236
Maprs779805236
PheGenIrs779805236
Biobankrs779805236
1000 genomesrs779805236
hgdprs779805236
ensemblrs779805236
geneviewrs779805236
scholarrs779805236
googlers779805236
pharmgkbrs779805236
gwascentralrs779805236
openSNPrs779805236
23andMers779805236
23andMe allrs779805236
SNPshotrs779805236
SNPdbers779805236
MSV3drs779805236
GWAS Ctlgrs779805236
Max Magnitude0
ClinVar
Risk rs779805236(G;G)
Alt rs779805236(G;G)
Reference Rs779805236(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene AFG3L2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.12370846A>G
CLNSRC
CLNACC RCV000482350.1,