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rs199683937

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199683937(A;C)
Make rs199683937(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position67611982
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs199683937
dbSNP (old)rs199683937
ClinGenrs199683937
ebirs199683937
HLIrs199683937
Exacrs199683937
Gnomadrs199683937
Varsomers199683937
Maprs199683937
PheGenIrs199683937
Biobankrs199683937
1000 genomesrs199683937
hgdprs199683937
ensemblrs199683937
gopubmedrs199683937
geneviewrs199683937
scholarrs199683937
googlers199683937
pharmgkbrs199683937
gwascentralrs199683937
openSNPrs199683937
23andMers199683937
23andMe allrs199683937
SNPshotrs199683937
SNPdbers199683937
MSV3drs199683937
GWAS Ctlgrs199683937
Max Magnitude0
ClinVar
Risk rs199683937(C;C)
Alt rs199683937(C;C)
Reference Rs199683937(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFV1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67379453A>C
CLNSRC
CLNACC RCV000414504.1,