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rs794726691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCTG;GCTG) 0 common in clinvar
Make rs794726691(-;-)
Make rs794726691(-;GGCT)
Make rs794726691(GGCT;GGCT)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position16006493
GeneTTC19
is asnp
is mentioned by
dbSNPrs794726691
dbSNP (old)rs794726691
ClinGenrs794726691
ebirs794726691
HLIrs794726691
Exacrs794726691
Gnomadrs794726691
Varsomers794726691
Maprs794726691
PheGenIrs794726691
Biobankrs794726691
1000 genomesrs794726691
hgdprs794726691
ensemblrs794726691
gopubmedrs794726691
geneviewrs794726691
scholarrs794726691
googlers794726691
pharmgkbrs794726691
gwascentralrs794726691
openSNPrs794726691
23andMers794726691
23andMe allrs794726691
SNP Nexus

SNPshotrs794726691
SNPdbers794726691
MSV3drs794726691
GWAS Ctlgrs794726691
Max Magnitude0
ClinVar
Risk rs794726691(-;-)
Alt rs794726691(-;-)
Reference Rs794726691(GCTG;GCTG)
Significance Pathogenic
Disease Mitochondrial complex III deficiency not provided
Variation info
Gene TTC19
CLNDBN Mitochondrial complex III deficiency, nuclear type 2 not provided
Reversed 0
HGVS NC_000017.10:g.15909807_15909810delGGCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000088675.3, RCV000201515.1,