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rs876657643

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs876657643(-;-)
Make rs876657643(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position76491684
GeneESRRB, LOC105370574
is asnp
is mentioned by
dbSNPrs876657643
ebirs876657643
HLIrs876657643
Exacrs876657643
Varsomers876657643
Maprs876657643
PheGenIrs876657643
hapmaprs876657643
1000 genomesrs876657643
hgdprs876657643
ensemblrs876657643
gopubmedrs876657643
geneviewrs876657643
scholarrs876657643
googlers876657643
pharmgkbrs876657643
gwascentralrs876657643
openSNPrs876657643
23andMers876657643
23andMe allrs876657643
SNP Nexus

SNPshotrs876657643
SNPdbers876657643
MSV3drs876657643
GWAS Ctlgrs876657643
Max Magnitude0
ClinVar
Risk rs876657643(;)
Alt rs876657643(;)
Reference rs876657643(TG;TG)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene ESRRB
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000014.8:g.76958027_76958028delTG
CLNSRC
CLNACC RCV000218592.1,