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rs751879424

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs751879424(-;-)
Make rs751879424(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position63617339
GeneDPY19L2
is asnp
is mentioned by
dbSNPrs751879424
ebirs751879424
HLIrs751879424
Exacrs751879424
Varsomers751879424
Maprs751879424
PheGenIrs751879424
hapmaprs751879424
1000 genomesrs751879424
hgdprs751879424
ensemblrs751879424
gopubmedrs751879424
geneviewrs751879424
scholarrs751879424
googlers751879424
pharmgkbrs751879424
gwascentralrs751879424
openSNPrs751879424
23andMers751879424
23andMe allrs751879424
SNP Nexus

SNPshotrs751879424
SNPdbers751879424
MSV3drs751879424
GWAS Ctlgrs751879424
Max Magnitude0
ClinVar
Risk rs751879424(;)
Alt rs751879424(;)
Reference rs751879424(A;A)
Significance Pathogenic
Disease Spermatogenic failure 9
Variation info
Gene DPY19L2
CLNDBN Spermatogenic failure 9
Reversed 0
HGVS NC_000012.11:g.64011119delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000087743.3,