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rs876657723

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657723(-;-)
Make rs876657723(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position107710188
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs876657723
ebirs876657723
HLIrs876657723
Exacrs876657723
Varsomers876657723
Maprs876657723
PheGenIrs876657723
hapmaprs876657723
1000 genomesrs876657723
hgdprs876657723
ensemblrs876657723
gopubmedrs876657723
geneviewrs876657723
scholarrs876657723
googlers876657723
pharmgkbrs876657723
gwascentralrs876657723
openSNPrs876657723
23andMers876657723
23andMe allrs876657723
SNP Nexus

SNPshotrs876657723
SNPdbers876657723
MSV3drs876657723
GWAS Ctlgrs876657723
Max Magnitude0
ClinVar
Risk rs876657723(;)
Alt rs876657723(;)
Reference rs876657723(A;A)
Significance Pathogenic
Disease Enlarged vestibular aqueduct syndrome Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Enlarged vestibular aqueduct syndrome Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107350633delA
CLNSRC
CLNACC RCV000221940.1,