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

rs747661849

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747661849(A;A)
Make rs747661849(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67609576
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs747661849
ebirs747661849
HLIrs747661849
Exacrs747661849
Varsomers747661849
Maprs747661849
PheGenIrs747661849
hapmaprs747661849
1000 genomesrs747661849
hgdprs747661849
ensemblrs747661849
gopubmedrs747661849
geneviewrs747661849
scholarrs747661849
googlers747661849
pharmgkbrs747661849
gwascentralrs747661849
openSNPrs747661849
23andMers747661849
23andMe allrs747661849
SNP Nexus

SNPshotrs747661849
SNPdbers747661849
MSV3drs747661849
GWAS Ctlgrs747661849
Max Magnitude0
ClinVar
Risk rs747661849(A;A)
Alt rs747661849(A;A)
Reference rs747661849(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFV1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67377047G>A
CLNSRC
CLNACC RCV000195585.1,