Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777205

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777205(A;A)
Make rs587777205(A;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position63569312
GeneDPY19L2
is asnp
is mentioned by
dbSNPrs587777205
ebirs587777205
HLIrs587777205
Exacrs587777205
Varsomers587777205
Maprs587777205
PheGenIrs587777205
hapmaprs587777205
1000 genomesrs587777205
hgdprs587777205
ensemblrs587777205
gopubmedrs587777205
geneviewrs587777205
scholarrs587777205
googlers587777205
pharmgkbrs587777205
gwascentralrs587777205
openSNPrs587777205
23andMers587777205
23andMe allrs587777205
SNP Nexus

SNPshotrs587777205
SNPdbers587777205
MSV3drs587777205
GWAS Ctlgrs587777205
Max Magnitude0
ClinVar
Risk rs587777205(A,G;A,G)
Alt rs587777205(A,G;A,G)
Reference rs587777205(T;T)
Significance Pathogenic
Disease Spermatogenic failure 9
Variation info
Gene DPY19L2
CLNDBN Spermatogenic failure 9
Reversed 0
HGVS NC_000012.11:g.63963092T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087742.3,