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rs121909111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909111(G;T)
Make rs121909111(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position76491683
GeneESRRB
is asnp
is mentioned by
dbSNPrs121909111
ebirs121909111
HLIrs121909111
Exacrs121909111
Varsomers121909111
Maprs121909111
PheGenIrs121909111
hapmaprs121909111
1000 genomesrs121909111
hgdprs121909111
ensemblrs121909111
gopubmedrs121909111
geneviewrs121909111
scholarrs121909111
googlers121909111
pharmgkbrs121909111
gwascentralrs121909111
openSNPrs121909111
23andMers121909111
23andMe allrs121909111
SNP Nexus

SNPshotrs121909111
SNPdbers121909111
MSV3drs121909111
GWAS Ctlgrs121909111
Max Magnitude0
OMIM602167
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909111(T;T)
Alt rs121909111(T;T)
Reference rs121909111(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene ESRRB
CLNDBN Deafness, autosomal recessive 35
Reversed 0
HGVS NC_000014.8:g.76958026G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007929.3,