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rs143246552

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs143246552(C;C)
Make rs143246552(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70853093
GeneTEX11
is asnp
is mentioned by
dbSNPrs143246552
ebirs143246552
HLIrs143246552
Exacrs143246552
Varsomers143246552
Maprs143246552
PheGenIrs143246552
hapmaprs143246552
1000 genomesrs143246552
hgdprs143246552
ensemblrs143246552
gopubmedrs143246552
geneviewrs143246552
scholarrs143246552
googlers143246552
pharmgkbrs143246552
gwascentralrs143246552
openSNPrs143246552
23andMers143246552
23andMe allrs143246552
SNP Nexus

SNPshotrs143246552
SNPdbers143246552
MSV3drs143246552
GWAS Ctlgrs143246552
Max Magnitude0
ClinVar
Risk rs143246552(C;C)
Alt rs143246552(C;C)
Reference rs143246552(T;T)
Significance Pathogenic
Disease Spermatogenic failure
Variation info
Gene TEX11
CLNDBN Spermatogenic failure, X-linked, 2
Reversed 0
HGVS NC_000023.10:g.70072943T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000173008.2,