Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057520369

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520369(C;C)
Make rs1057520369(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107694404
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1057520369
dbSNP (old)rs1057520369
ClinGenrs1057520369
ebirs1057520369
HLIrs1057520369
Exacrs1057520369
Gnomadrs1057520369
Varsomers1057520369
Maprs1057520369
PheGenIrs1057520369
Biobankrs1057520369
1000 genomesrs1057520369
hgdprs1057520369
ensemblrs1057520369
gopubmedrs1057520369
geneviewrs1057520369
scholarrs1057520369
googlers1057520369
pharmgkbrs1057520369
gwascentralrs1057520369
openSNPrs1057520369
23andMers1057520369
23andMe allrs1057520369
SNPshotrs1057520369
SNPdbers1057520369
MSV3drs1057520369
GWAS Ctlgrs1057520369
Max Magnitude0
ClinVar
Risk rs1057520369(C;C)
Alt rs1057520369(C;C)
Reference Rs1057520369(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC26A4
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107334849T>C
CLNSRC
CLNACC RCV000417941.1,