Have questions? Visit https://www.reddit.com/r/SNPedia

rs767298430

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs767298430(-;-)
Make rs767298430(-;G)
Make rs767298430(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position83284866
GeneCOQ2
is asnp
is mentioned by
dbSNPrs767298430
ebirs767298430
HLIrs767298430
Exacrs767298430
Varsomers767298430
Maprs767298430
PheGenIrs767298430
hapmaprs767298430
1000 genomesrs767298430
hgdprs767298430
ensemblrs767298430
gopubmedrs767298430
geneviewrs767298430
scholarrs767298430
googlers767298430
pharmgkbrs767298430
gwascentralrs767298430
openSNPrs767298430
23andMers767298430
23andMe allrs767298430
SNP Nexus

SNPshotrs767298430
SNPdbers767298430
MSV3drs767298430
GWAS Ctlgrs767298430
Max Magnitude0
ClinVar
Risk rs767298430(G;G)
Alt rs767298430(G;G)
Reference rs767298430(;)
Significance Pathogenic
Disease not provided
Variation info
Gene COQ2
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.84206020dupG
CLNSRC
CLNACC RCV000224356.1,