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

rs767122069

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767122069(C;T)
Make rs767122069(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position206124262
GeneNDUFS1
is asnp
is mentioned by
dbSNPrs767122069
ebirs767122069
HLIrs767122069
Exacrs767122069
Varsomers767122069
Maprs767122069
PheGenIrs767122069
hapmaprs767122069
1000 genomesrs767122069
hgdprs767122069
ensemblrs767122069
gopubmedrs767122069
geneviewrs767122069
scholarrs767122069
googlers767122069
pharmgkbrs767122069
gwascentralrs767122069
openSNPrs767122069
23andMers767122069
23andMe allrs767122069
SNP Nexus

SNPshotrs767122069
SNPdbers767122069
MSV3drs767122069
GWAS Ctlgrs767122069
Max Magnitude0
ClinVar
Risk rs767122069(T;T)
Alt rs767122069(T;T)
Reference rs767122069(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.206988986C>T
CLNSRC
CLNACC RCV000199572.2,