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rs761785906

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761785906(A;A)
Make rs761785906(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position83267737
GeneCOQ2
is asnp
is mentioned by
dbSNPrs761785906
ebirs761785906
HLIrs761785906
Exacrs761785906
Varsomers761785906
Maprs761785906
PheGenIrs761785906
hapmaprs761785906
1000 genomesrs761785906
hgdprs761785906
ensemblrs761785906
gopubmedrs761785906
geneviewrs761785906
scholarrs761785906
googlers761785906
pharmgkbrs761785906
gwascentralrs761785906
openSNPrs761785906
23andMers761785906
23andMe allrs761785906
SNP Nexus

SNPshotrs761785906
SNPdbers761785906
MSV3drs761785906
GWAS Ctlgrs761785906
Max Magnitude0
ClinVar
Risk rs761785906(A;A)
Alt rs761785906(A;A)
Reference rs761785906(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COQ2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.84188890G>A
CLNSRC
CLNACC RCV000195593.1,