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rs150667550

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs150667550(C;C)
Make rs150667550(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161210599
GeneNDUFS2
is asnp
is mentioned by
dbSNPrs150667550
ebirs150667550
HLIrs150667550
Exacrs150667550
Varsomers150667550
Maprs150667550
PheGenIrs150667550
hapmaprs150667550
1000 genomesrs150667550
hgdprs150667550
ensemblrs150667550
gopubmedrs150667550
geneviewrs150667550
scholarrs150667550
googlers150667550
pharmgkbrs150667550
gwascentralrs150667550
openSNPrs150667550
23andMers150667550
23andMe allrs150667550
SNP Nexus

SNPshotrs150667550
SNPdbers150667550
MSV3drs150667550
GWAS Ctlgrs150667550
Max Magnitude0
ClinVar
Risk rs150667550(C;C)
Alt rs150667550(C;C)
Reference rs150667550(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFS2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.161180389T>C
CLNSRC
CLNACC RCV000198967.1,