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rs140984555

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140984555(C;T)
Make rs140984555(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70605421
GeneTEX11
is asnp
is mentioned by
dbSNPrs140984555
ebirs140984555
HLIrs140984555
Exacrs140984555
Varsomers140984555
Maprs140984555
PheGenIrs140984555
hapmaprs140984555
1000 genomesrs140984555
hgdprs140984555
ensemblrs140984555
gopubmedrs140984555
geneviewrs140984555
scholarrs140984555
googlers140984555
pharmgkbrs140984555
gwascentralrs140984555
openSNPrs140984555
23andMers140984555
23andMe allrs140984555
SNP Nexus

SNPshotrs140984555
SNPdbers140984555
MSV3drs140984555
GWAS Ctlgrs140984555
Max Magnitude0
ClinVar
Risk rs140984555(T;T)
Alt rs140984555(T;T)
Reference rs140984555(C;C)
Significance Pathogenic
Disease Spermatogenic failure
Variation info
Gene TEX11
CLNDBN Spermatogenic failure, X-linked, 2
Reversed 0
HGVS NC_000023.10:g.69825271C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000173009.2,