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

rs1057521147

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521147(A;A)
Make rs1057521147(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107696044
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1057521147
dbSNP (old)rs1057521147
ClinGenrs1057521147
ebirs1057521147
HLIrs1057521147
Exacrs1057521147
Gnomadrs1057521147
Varsomers1057521147
Maprs1057521147
PheGenIrs1057521147
Biobankrs1057521147
1000 genomesrs1057521147
hgdprs1057521147
ensemblrs1057521147
gopubmedrs1057521147
geneviewrs1057521147
scholarrs1057521147
googlers1057521147
pharmgkbrs1057521147
gwascentralrs1057521147
openSNPrs1057521147
23andMers1057521147
23andMe allrs1057521147
SNPshotrs1057521147
SNPdbers1057521147
MSV3drs1057521147
GWAS Ctlgrs1057521147
Max Magnitude0
ClinVar
Risk rs1057521147(A;A)
Alt rs1057521147(A;A)
Reference Rs1057521147(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC26A4
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107336489G>A
CLNSRC
CLNACC RCV000431089.1,