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rs868256749

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs868256749(C;T)
Make rs868256749(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position63617303
GeneDPY19L2
is asnp
is mentioned by
dbSNPrs868256749
ebirs868256749
HLIrs868256749
Exacrs868256749
Varsomers868256749
Maprs868256749
PheGenIrs868256749
hapmaprs868256749
1000 genomesrs868256749
hgdprs868256749
ensemblrs868256749
gopubmedrs868256749
geneviewrs868256749
scholarrs868256749
googlers868256749
pharmgkbrs868256749
gwascentralrs868256749
openSNPrs868256749
23andMers868256749
23andMe allrs868256749
SNP Nexus

SNPshotrs868256749
SNPdbers868256749
MSV3drs868256749
GWAS Ctlgrs868256749
Max Magnitude0
ClinVar
Risk rs868256749(T;T)
Alt rs868256749(T;T)
Reference rs868256749(C;C)
Significance Pathogenic
Disease Spermatogenic failure 9
Variation info
Gene DPY19L2
CLNDBN Spermatogenic failure 9
Reversed 0
HGVS NC_000012.11:g.64011083C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087746.3,