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rs147088100

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147088100(A;A)
Make rs147088100(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position70853248
GeneTEX11
is asnp
is mentioned by
dbSNPrs147088100
ebirs147088100
HLIrs147088100
Exacrs147088100
Varsomers147088100
Maprs147088100
PheGenIrs147088100
hapmaprs147088100
1000 genomesrs147088100
hgdprs147088100
ensemblrs147088100
gopubmedrs147088100
geneviewrs147088100
scholarrs147088100
googlers147088100
pharmgkbrs147088100
gwascentralrs147088100
openSNPrs147088100
23andMers147088100
23andMe allrs147088100
SNP Nexus

SNPshotrs147088100
SNPdbers147088100
MSV3drs147088100
GWAS Ctlgrs147088100
Max Magnitude0
ClinVar
Risk rs147088100(A;A)
Alt rs147088100(A;A)
Reference rs147088100(G;G)
Significance Pathogenic
Disease Spermatogenic failure
Variation info
Gene TEX11
CLNDBN Spermatogenic failure, X-linked, 2
Reversed 0
HGVS NC_000023.10:g.70073098G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000173010.2,