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rs118192103

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118192103(A;A)
Make rs118192103(A;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position8342
GeneFAM160B1
is asnp
is mentioned by
dbSNPrs118192103
ebirs118192103
HLIrs118192103
Exacrs118192103
Varsomers118192103
Maprs118192103
PheGenIrs118192103
hapmaprs118192103
1000 genomesrs118192103
hgdprs118192103
ensemblrs118192103
gopubmedrs118192103
geneviewrs118192103
scholarrs118192103
googlers118192103
pharmgkbrs118192103
gwascentralrs118192103
openSNPrs118192103
23andMers118192103
23andMe allrs118192103
SNP Nexus

SNPshotrs118192103
SNPdbers118192103
MSV3drs118192103
GWAS Ctlgrs118192103
Max Magnitude0
ClinVar
Risk rs118192103(A;A)
Alt rs118192103(A;A)
Reference rs118192103(G;G)
Significance Pathogenic
Disease Progressive external ophthalmoplegia with myoclonus not specified
Variation info
Gene
CLNDBN Progressive external ophthalmoplegia with myoclonus not specified
Reversed 0
HGVS NC_012920.1:m.8342G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010198.3, RCV000223829.1,