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rs587777206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777206(A;A)
Make rs587777206(A;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position63624101
GeneDPY19L2
is asnp
is mentioned by
dbSNPrs587777206
ebirs587777206
HLIrs587777206
Exacrs587777206
Varsomers587777206
Maprs587777206
PheGenIrs587777206
hapmaprs587777206
1000 genomesrs587777206
hgdprs587777206
ensemblrs587777206
gopubmedrs587777206
geneviewrs587777206
scholarrs587777206
googlers587777206
pharmgkbrs587777206
gwascentralrs587777206
openSNPrs587777206
23andMers587777206
23andMe allrs587777206
SNP Nexus

SNPshotrs587777206
SNPdbers587777206
MSV3drs587777206
GWAS Ctlgrs587777206
Max Magnitude0
ClinVar
Risk rs587777206(A,G;A,G)
Alt rs587777206(A,G;A,G)
Reference rs587777206(C;C)
Significance Pathogenic
Disease Spermatogenic failure 9
Variation info
Gene DPY19L2
CLNDBN Spermatogenic failure 9
Reversed 1
HGVS NC_000012.11:g.64017881G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000087745.3,