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rs118192102

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118192102(A;G)
Make rs118192102(G;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position8296
GeneFAM160B1
is asnp
is mentioned by
dbSNPrs118192102
ebirs118192102
HLIrs118192102
Exacrs118192102
Varsomers118192102
Maprs118192102
PheGenIrs118192102
hapmaprs118192102
1000 genomesrs118192102
hgdprs118192102
ensemblrs118192102
gopubmedrs118192102
geneviewrs118192102
scholarrs118192102
googlers118192102
pharmgkbrs118192102
gwascentralrs118192102
openSNPrs118192102
23andMers118192102
23andMe allrs118192102
SNP Nexus

SNPshotrs118192102
SNPdbers118192102
MSV3drs118192102
GWAS Ctlgrs118192102
Max Magnitude0
ClinVar
Risk rs118192102(G;G)
Alt rs118192102(G;G)
Reference rs118192102(A;A)
Significance Pathogenic
Disease Diabetes-deafness syndrome maternally transmitted
Variation info
Gene
CLNDBN Diabetes-deafness syndrome maternally transmitted
Reversed 0
HGVS NC_012920.1:m.8296A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010201.3,