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rs398123027

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123027(C;T)
Make rs398123027(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position35943953
GeneSLC26A8
is asnp
is mentioned by
dbSNPrs398123027
ebirs398123027
HLIrs398123027
Exacrs398123027
Varsomers398123027
Maprs398123027
PheGenIrs398123027
hapmaprs398123027
1000 genomesrs398123027
hgdprs398123027
ensemblrs398123027
gopubmedrs398123027
geneviewrs398123027
scholarrs398123027
googlers398123027
pharmgkbrs398123027
gwascentralrs398123027
openSNPrs398123027
23andMers398123027
23andMe allrs398123027
SNP Nexus

SNPshotrs398123027
SNPdbers398123027
MSV3drs398123027
GWAS Ctlgrs398123027
Max Magnitude0
ClinVar
Risk rs398123027(T;T)
Alt rs398123027(T;T)
Reference rs398123027(C;C)
Significance Pathogenic
Disease Spermatogenic failure 3
Variation info
Gene SLC26A8
CLNDBN Spermatogenic failure 3
Reversed 1
HGVS NC_000006.11:g.35911730G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043626.2,