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rs876657722

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657722(A;A)
Make rs876657722(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position107696040
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs876657722
ebirs876657722
HLIrs876657722
Exacrs876657722
Varsomers876657722
Maprs876657722
PheGenIrs876657722
hapmaprs876657722
1000 genomesrs876657722
hgdprs876657722
ensemblrs876657722
gopubmedrs876657722
geneviewrs876657722
scholarrs876657722
googlers876657722
pharmgkbrs876657722
gwascentralrs876657722
openSNPrs876657722
23andMers876657722
23andMe allrs876657722
SNP Nexus

SNPshotrs876657722
SNPdbers876657722
MSV3drs876657722
GWAS Ctlgrs876657722
Max Magnitude0
ClinVar
Risk rs876657722(A;A)
Alt rs876657722(A;A)
Reference Rs876657722(G;G)
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.107336485G>A
CLNSRC
CLNACC RCV000213351.1,