rs587777432

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AAAC;AAAC)	0	common in clinvar
(AACA;AACA)	0	common in clinvar
(I;I)	0	common genotype

Make rs587777432(-;-)

Make rs587777432(-;AACA)

Reference

GRCh38 38.1/142

Chromosome

17

Position

4744214

Gene

ZMYND15

is a	snp
is	mentioned by
dbSNP	rs587777432
dbSNP (classic)	rs587777432
ClinGen	rs587777432
ebi	rs587777432
HLI	rs587777432
Exac	rs587777432
Gnomad	rs587777432
Varsome	rs587777432
LitVar	rs587777432
Map	rs587777432
PheGenI	rs587777432
Biobank	rs587777432
1000 genomes	rs587777432
hgdp	rs587777432
ensembl	rs587777432
geneview	rs587777432
scholar	rs587777432
google	rs587777432
pharmgkb	rs587777432
gwascentral	rs587777432
openSNP	rs587777432
23andMe	rs587777432
SNPshot	rs587777432
SNPdbe	rs587777432
MSV3d	rs587777432
GWAS Ctlg	rs587777432

Max Magnitude

0

ClinVar
Risk	rs587777432(-;-) Rs587777432(AAAC;AAAC)
Alt	rs587777432(-;-) Rs587777432(AAAC;AAAC)
Reference	Rs587777432(AACA;AACA)
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,