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rs61742642

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61742642(C;T)
Make rs61742642(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position76498312
GeneESRRB, LOC105370574
is asnp
is mentioned by
dbSNPrs61742642
ebirs61742642
HLIrs61742642
Exacrs61742642
Varsomers61742642
Maprs61742642
PheGenIrs61742642
hapmaprs61742642
1000 genomesrs61742642
hgdprs61742642
ensemblrs61742642
gopubmedrs61742642
geneviewrs61742642
scholarrs61742642
googlers61742642
pharmgkbrs61742642
gwascentralrs61742642
openSNPrs61742642
23andMers61742642
23andMe allrs61742642
SNP Nexus

SNPshotrs61742642
SNPdbers61742642
MSV3drs61742642
GWAS Ctlgrs61742642
Max Magnitude0

[PMID 25938503] Feasibility of a bilateral 4000-6000 Hz notch as a phenotype for genetic association analysis.

ClinVar
Risk rs61742642(A,T;A,T)
Alt rs61742642(A,T;A,T)
Reference rs61742642(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ESRRB
CLNDBN not specified
Reversed 0
HGVS NC_000014.8:g.76964655C>T
CLNSRC
CLNACC RCV000038134.2,