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rs876657644

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657644(A;C)
Make rs876657644(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position133461112
GeneEYA4
is asnp
is mentioned by
dbSNPrs876657644
ebirs876657644
HLIrs876657644
Exacrs876657644
Varsomers876657644
Maprs876657644
PheGenIrs876657644
hapmaprs876657644
1000 genomesrs876657644
hgdprs876657644
ensemblrs876657644
gopubmedrs876657644
geneviewrs876657644
scholarrs876657644
googlers876657644
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gwascentralrs876657644
openSNPrs876657644
23andMers876657644
23andMe allrs876657644
SNP Nexus

SNPshotrs876657644
SNPdbers876657644
MSV3drs876657644
GWAS Ctlgrs876657644
Max Magnitude0
ClinVar
Risk rs876657644(C;C)
Alt rs876657644(C;C)
Reference rs876657644(A;A)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene EYA4 LOC101928164
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000006.11:g.133782250A>C
CLNSRC
CLNACC RCV000223505.1,