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rs757486575

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757486575(A;A)
Make rs757486575(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67609474
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs757486575
ebirs757486575
HLIrs757486575
Exacrs757486575
Varsomers757486575
Maprs757486575
PheGenIrs757486575
hapmaprs757486575
1000 genomesrs757486575
hgdprs757486575
ensemblrs757486575
gopubmedrs757486575
geneviewrs757486575
scholarrs757486575
googlers757486575
pharmgkbrs757486575
gwascentralrs757486575
openSNPrs757486575
23andMers757486575
23andMe allrs757486575
SNP Nexus

SNPshotrs757486575
SNPdbers757486575
MSV3drs757486575
GWAS Ctlgrs757486575
Max Magnitude0
ClinVar
Risk rs757486575(A;A)
Alt rs757486575(A;A)
Reference rs757486575(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFV1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67376945G>A
CLNSRC
CLNACC RCV000200734.1,