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rs567032648

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs567032648(C;C)
Make rs567032648(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position49022175
GeneDALRD3, MIR191, MIR425, NDUFAF3
is asnp
is mentioned by
dbSNPrs567032648
ebirs567032648
HLIrs567032648
Exacrs567032648
Varsomers567032648
Maprs567032648
PheGenIrs567032648
hapmaprs567032648
1000 genomesrs567032648
hgdprs567032648
ensemblrs567032648
gopubmedrs567032648
geneviewrs567032648
scholarrs567032648
googlers567032648
pharmgkbrs567032648
gwascentralrs567032648
openSNPrs567032648
23andMers567032648
23andMe allrs567032648
SNP Nexus

SNPshotrs567032648
SNPdbers567032648
MSV3drs567032648
GWAS Ctlgrs567032648
Max Magnitude0
ClinVar
Risk rs567032648(C,G;C,G)
Alt rs567032648(C,G;C,G)
Reference rs567032648(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR425 DALRD3 MIR191 NDUFAF3
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.49059608T>G
CLNSRC
CLNACC RCV000198139.1,