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rs140210148

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140210148(C;T)
Make rs140210148(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position36012301
GeneSLC26A8
is asnp
is mentioned by
dbSNPrs140210148
ebirs140210148
HLIrs140210148
Exacrs140210148
Varsomers140210148
Maprs140210148
PheGenIrs140210148
hapmaprs140210148
1000 genomesrs140210148
hgdprs140210148
ensemblrs140210148
gopubmedrs140210148
geneviewrs140210148
scholarrs140210148
googlers140210148
pharmgkbrs140210148
gwascentralrs140210148
openSNPrs140210148
23andMers140210148
23andMe allrs140210148
SNP Nexus

SNPshotrs140210148
SNPdbers140210148
MSV3drs140210148
GWAS Ctlgrs140210148
Max Magnitude0
ClinVar
Risk rs140210148(T;T)
Alt rs140210148(T;T)
Reference rs140210148(C;C)
Significance Pathogenic
Disease Spermatogenic failure 3
Variation info
Gene SLC26A8
CLNDBN Spermatogenic failure 3
Reversed 0
HGVS NC_000006.11:g.35980078C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043624.2,