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rs1057518810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518810(C;C)
Make rs1057518810(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107663430
GeneSLC26A4, SLC26A4-AS1
is asnp
is mentioned by
dbSNPrs1057518810
dbSNP (old)rs1057518810
ClinGenrs1057518810
ebirs1057518810
HLIrs1057518810
Exacrs1057518810
Gnomadrs1057518810
Varsomers1057518810
LitVarrs1057518810
Maprs1057518810
PheGenIrs1057518810
Biobankrs1057518810
1000 genomesrs1057518810
hgdprs1057518810
ensemblrs1057518810
gopubmedrs1057518810
geneviewrs1057518810
scholarrs1057518810
googlers1057518810
pharmgkbrs1057518810
gwascentralrs1057518810
openSNPrs1057518810
23andMers1057518810
23andMe allrs1057518810
SNPshotrs1057518810
SNPdbers1057518810
MSV3drs1057518810
GWAS Ctlgrs1057518810
Max Magnitude0
ClinVar
Risk rs1057518810(C;C)
Alt rs1057518810(C;C)
Reference Rs1057518810(T;T)
Significance Probable-Pathogenic
Disease Hearing impairment
Variation info
Gene SLC26A4-AS1 SLC26A4
CLNDBN Hearing impairment
Reversed 0
HGVS NC_000007.13:g.107303875T>C
CLNSRC
CLNACC RCV000414878.1,