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rs752807925

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752807925(C;T)
Make rs752807925(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position107704382
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs752807925
ebirs752807925
HLIrs752807925
Exacrs752807925
Varsomers752807925
Maprs752807925
PheGenIrs752807925
hapmaprs752807925
1000 genomesrs752807925
hgdprs752807925
ensemblrs752807925
gopubmedrs752807925
geneviewrs752807925
scholarrs752807925
googlers752807925
pharmgkbrs752807925
gwascentralrs752807925
openSNPrs752807925
23andMers752807925
23andMe allrs752807925
SNP Nexus

SNPshotrs752807925
SNPdbers752807925
MSV3drs752807925
GWAS Ctlgrs752807925
Merged fromRs786204742
Max Magnitude0
ClinVar
Risk rs752807925(T;T)
Alt rs752807925(T;T)
Reference rs752807925(C;C)
Significance Probable-Pathogenic
Disease Pendred's syndrome
Variation info
Gene SLC26A4
CLNDBN Pendred's syndrome
Reversed 0
HGVS NC_000007.13:g.107344827C>T
CLNSRC
CLNACC RCV000169591.1,