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rs146281367

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146281367(A;A)
Make rs146281367(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position107683537
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs146281367
ebirs146281367
HLIrs146281367
Exacrs146281367
Varsomers146281367
Maprs146281367
PheGenIrs146281367
hapmaprs146281367
1000 genomesrs146281367
hgdprs146281367
ensemblrs146281367
gopubmedrs146281367
geneviewrs146281367
scholarrs146281367
googlers146281367
pharmgkbrs146281367
gwascentralrs146281367
openSNPrs146281367
23andMers146281367
23andMe allrs146281367
SNP Nexus

SNPshotrs146281367
SNPdbers146281367
MSV3drs146281367
GWAS Ctlgrs146281367
Max Magnitude0
ClinVar
Risk rs146281367(A,C,T;A,C,T)
Alt rs146281367(A,C,T;A,C,T)
Reference rs146281367(G;G)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107323982G>T
CLNSRC
CLNACC RCV000169430.1,