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rs1057524176

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524176(C;T)
Make rs1057524176(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107710170
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1057524176
dbSNP (old)rs1057524176
ClinGenrs1057524176
ebirs1057524176
HLIrs1057524176
Exacrs1057524176
Gnomadrs1057524176
Varsomers1057524176
Maprs1057524176
PheGenIrs1057524176
Biobankrs1057524176
1000 genomesrs1057524176
hgdprs1057524176
ensemblrs1057524176
gopubmedrs1057524176
geneviewrs1057524176
scholarrs1057524176
googlers1057524176
pharmgkbrs1057524176
gwascentralrs1057524176
openSNPrs1057524176
23andMers1057524176
23andMe allrs1057524176
SNPshotrs1057524176
SNPdbers1057524176
MSV3drs1057524176
GWAS Ctlgrs1057524176
Max Magnitude0
ClinVar
Risk rs1057524176(T;T)
Alt rs1057524176(T;T)
Reference Rs1057524176(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC26A4
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107350615C>T
CLNSRC
CLNACC RCV000426133.1,