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rs142724470

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs142724470(C;T)
Make rs142724470(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position35951201
GeneSLC26A8
is asnp
is mentioned by
dbSNPrs142724470
ebirs142724470
HLIrs142724470
Exacrs142724470
Varsomers142724470
Maprs142724470
PheGenIrs142724470
hapmaprs142724470
1000 genomesrs142724470
hgdprs142724470
ensemblrs142724470
gopubmedrs142724470
geneviewrs142724470
scholarrs142724470
googlers142724470
pharmgkbrs142724470
gwascentralrs142724470
openSNPrs142724470
23andMers142724470
23andMe allrs142724470
SNP Nexus

SNPshotrs142724470
SNPdbers142724470
MSV3drs142724470
GWAS Ctlgrs142724470
Max Magnitude0
ClinVar
Risk rs142724470(T;T)
Alt rs142724470(T;T)
Reference rs142724470(C;C)
Significance Pathogenic
Disease Spermatogenic failure 3
Variation info
Gene SLC26A8
CLNDBN Spermatogenic failure 3
Reversed 0
HGVS NC_000006.11:g.35918978C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043625.2,