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rs147579680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs147579680(C;T)
Make rs147579680(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position63624124
GeneDPY19L2
is asnp
is mentioned by
dbSNPrs147579680
ebirs147579680
HLIrs147579680
Exacrs147579680
Varsomers147579680
Maprs147579680
PheGenIrs147579680
hapmaprs147579680
1000 genomesrs147579680
hgdprs147579680
ensemblrs147579680
gopubmedrs147579680
geneviewrs147579680
scholarrs147579680
googlers147579680
pharmgkbrs147579680
gwascentralrs147579680
openSNPrs147579680
23andMers147579680
23andMe allrs147579680
SNP Nexus

SNPshotrs147579680
SNPdbers147579680
MSV3drs147579680
GWAS Ctlgrs147579680
Max Magnitude0
ClinVar
Risk rs147579680(T;T)
Alt rs147579680(T;T)
Reference rs147579680(C;C)
Significance Pathogenic
Disease Spermatogenic failure 9
Variation info
Gene DPY19L2
CLNDBN Spermatogenic failure 9
Reversed 0
HGVS NC_000012.11:g.64017904C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087741.3,