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rs371040282

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs371040282(A;G)
Make rs371040282(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position9124973
GeneNDUFV2, NDUFV2-AS1
is asnp
is mentioned by
dbSNPrs371040282
ebirs371040282
HLIrs371040282
Exacrs371040282
Varsomers371040282
Maprs371040282
PheGenIrs371040282
hapmaprs371040282
1000 genomesrs371040282
hgdprs371040282
ensemblrs371040282
gopubmedrs371040282
geneviewrs371040282
scholarrs371040282
googlers371040282
pharmgkbrs371040282
gwascentralrs371040282
openSNPrs371040282
23andMers371040282
23andMe allrs371040282
SNP Nexus

SNPshotrs371040282
SNPdbers371040282
MSV3drs371040282
GWAS Ctlgrs371040282
Max Magnitude0
ClinVar
Risk rs371040282(G;G)
Alt rs371040282(G;G)
Reference rs371040282(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFV2-AS1 RP11-143J12.2 LOC101927275 NDUFV2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.9124971A>G
CLNSRC
CLNACC RCV000198608.1,