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rs772037717

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs772037717(A;G)
Make rs772037717(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position98875675
GeneFBXL4
is asnp
is mentioned by
dbSNPrs772037717
ebirs772037717
HLIrs772037717
Exacrs772037717
Varsomers772037717
Maprs772037717
PheGenIrs772037717
hapmaprs772037717
1000 genomesrs772037717
hgdprs772037717
ensemblrs772037717
gopubmedrs772037717
geneviewrs772037717
scholarrs772037717
googlers772037717
pharmgkbrs772037717
gwascentralrs772037717
openSNPrs772037717
23andMers772037717
23andMe allrs772037717
SNP Nexus

SNPshotrs772037717
SNPdbers772037717
MSV3drs772037717
GWAS Ctlgrs772037717
Max Magnitude0
ClinVar
Risk rs772037717(G;G)
Alt rs772037717(G;G)
Reference rs772037717(A;A)
Significance Probable-Pathogenic
Disease Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)
Variation info
Gene FBXL4
CLNDBN Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)
Reversed 0
HGVS NC_000006.11:g.99323551A>G
CLNSRC
CLNACC RCV000223958.1,