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rs750831299

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs750831299(C;T)
Make rs750831299(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67609490
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs750831299
ebirs750831299
HLIrs750831299
Exacrs750831299
Varsomers750831299
Maprs750831299
PheGenIrs750831299
hapmaprs750831299
1000 genomesrs750831299
hgdprs750831299
ensemblrs750831299
gopubmedrs750831299
geneviewrs750831299
scholarrs750831299
googlers750831299
pharmgkbrs750831299
gwascentralrs750831299
openSNPrs750831299
23andMers750831299
23andMe allrs750831299
SNP Nexus

SNPshotrs750831299
SNPdbers750831299
MSV3drs750831299
GWAS Ctlgrs750831299
Max Magnitude0
ClinVar
Risk rs750831299(T;T)
Alt rs750831299(T;T)
Reference rs750831299(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFV1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67376961C>T
CLNSRC
CLNACC RCV000197256.1,