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rs1057518006

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518006(A;A)
Make rs1057518006(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position107689136
GeneSLC26A4
is asnp
is mentioned by
dbSNPrs1057518006
dbSNP (old)rs1057518006
ClinGenrs1057518006
ebirs1057518006
HLIrs1057518006
Exacrs1057518006
Gnomadrs1057518006
Varsomers1057518006
Maprs1057518006
PheGenIrs1057518006
Biobankrs1057518006
1000 genomesrs1057518006
hgdprs1057518006
ensemblrs1057518006
gopubmedrs1057518006
geneviewrs1057518006
scholarrs1057518006
googlers1057518006
pharmgkbrs1057518006
gwascentralrs1057518006
openSNPrs1057518006
23andMers1057518006
23andMe allrs1057518006
SNPshotrs1057518006
SNPdbers1057518006
MSV3drs1057518006
GWAS Ctlgrs1057518006
Max Magnitude0
ClinVar
Risk rs1057518006(A;A)
Alt rs1057518006(A;A)
Reference Rs1057518006(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC26A4
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.107329581C>A
CLNSRC
CLNACC RCV000413685.1,