Have questions? Visit https://www.reddit.com/r/SNPedia

rs727503041

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503041(A;A)
Make rs727503041(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position76498317
GeneESRRB, LOC105370574
is asnp
is mentioned by
dbSNPrs727503041
ebirs727503041
HLIrs727503041
Exacrs727503041
Varsomers727503041
Maprs727503041
PheGenIrs727503041
hapmaprs727503041
1000 genomesrs727503041
hgdprs727503041
ensemblrs727503041
gopubmedrs727503041
geneviewrs727503041
scholarrs727503041
googlers727503041
pharmgkbrs727503041
gwascentralrs727503041
openSNPrs727503041
23andMers727503041
23andMe allrs727503041
SNP Nexus

SNPshotrs727503041
SNPdbers727503041
MSV3drs727503041
GWAS Ctlgrs727503041
Max Magnitude0
ClinVar
Risk rs727503041(A;A)
Alt rs727503041(A;A)
Reference rs727503041(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene ESRRB
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000014.8:g.76964660G>A
CLNSRC
CLNACC RCV000150664.1,