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

rs587777432

来自SNPedia
跳转至:导航搜索

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAC;AAAC) 0 common in clinvar
Make rs587777432(-;-)
Make rs587777432(-;AACA)
Make rs587777432(AACA;AACA)
ReferenceGRCh38 38.1/142
Chromosome17
Position4744214
GeneZMYND15
is asnp
is mentioned by
dbSNPrs587777432
ebirs587777432
HLIrs587777432
Exacrs587777432
Varsomers587777432
Maprs587777432
PheGenIrs587777432
hapmaprs587777432
1000 genomesrs587777432
hgdprs587777432
ensemblrs587777432
gopubmedrs587777432
geneviewrs587777432
scholarrs587777432
googlers587777432
pharmgkbrs587777432
gwascentralrs587777432
openSNPrs587777432
23andMers587777432
23andMe allrs587777432
SNP Nexus

SNPshotrs587777432
SNPdbers587777432
MSV3drs587777432
GWAS Ctlgrs587777432
Max Magnitude0
ClinVar
Risk rs587777432(;)
Alt rs587777432(;)
Reference rs587777432(AAAC;AAAC)
Significance Pathogenic
Disease Spermatogenic failure 14
Variation info
Gene ZMYND15
CLNDBN Spermatogenic failure 14
Reversed 0
HGVS NC_000017.10:g.4647509_4647512delAACA
CLNSRC OMIM Allelic Variant
CLNACC RCV000122741.3,