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rs150966634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150966634(C;T)
Make rs150966634(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position67611972
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs150966634
dbSNP (old)rs150966634
ClinGenrs150966634
ebirs150966634
HLIrs150966634
Exacrs150966634
Gnomadrs150966634
Varsomers150966634
Maprs150966634
PheGenIrs150966634
Biobankrs150966634
1000 genomesrs150966634
hgdprs150966634
ensemblrs150966634
gopubmedrs150966634
geneviewrs150966634
scholarrs150966634
googlers150966634
pharmgkbrs150966634
gwascentralrs150966634
openSNPrs150966634
23andMers150966634
23andMe allrs150966634
SNPshotrs150966634
SNPdbers150966634
MSV3drs150966634
GWAS Ctlgrs150966634
Max Magnitude0
ClinVar
Risk rs150966634(T;T)
Alt rs150966634(T;T)
Reference Rs150966634(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFV1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67379443C>T
CLNSRC
CLNACC RCV000482108.1,