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rs587777427

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777427(C;T)
Make rs587777427(T;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position26293530
GeneTAF4B
is asnp
is mentioned by
dbSNPrs587777427
ebirs587777427
HLIrs587777427
Exacrs587777427
Varsomers587777427
Maprs587777427
PheGenIrs587777427
hapmaprs587777427
1000 genomesrs587777427
hgdprs587777427
ensemblrs587777427
gopubmedrs587777427
geneviewrs587777427
scholarrs587777427
googlers587777427
pharmgkbrs587777427
gwascentralrs587777427
openSNPrs587777427
23andMers587777427
23andMe allrs587777427
SNP Nexus

SNPshotrs587777427
SNPdbers587777427
MSV3drs587777427
GWAS Ctlgrs587777427
Max Magnitude0
ClinVar
Risk rs587777427(T;T)
Alt rs587777427(T;T)
Reference rs587777427(C;C)
Significance Pathogenic
Disease Spermatogenic failure 13
Variation info
Gene TAF4B
CLNDBN Spermatogenic failure 13
Reversed 0
HGVS NC_000018.9:g.23873494C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000122735.2,