rs587777230

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs587777230(A;A)

Make rs587777230(A;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

196707811

Gene

CEP19

is a	snp
is	mentioned by
dbSNP	rs587777230
dbSNP (classic)	rs587777230
ClinGen	rs587777230
ebi	rs587777230
HLI	rs587777230
Exac	rs587777230
Gnomad	rs587777230
Varsome	rs587777230
LitVar	rs587777230
Map	rs587777230
PheGenI	rs587777230
Biobank	rs587777230
1000 genomes	rs587777230
hgdp	rs587777230
ensembl	rs587777230
geneview	rs587777230
scholar	rs587777230
google	rs587777230
pharmgkb	rs587777230
gwascentral	rs587777230
openSNP	rs587777230
23andMe	rs587777230
SNPshot	rs587777230
SNPdbe	rs587777230
MSV3d	rs587777230
GWAS Ctlg	rs587777230

Max Magnitude

0

ClinVar
Risk	rs587777230(A;A)
Alt	rs587777230(A;A)
Reference	Rs587777230(G;G)
Significance	Pathogenic
Disease	Morbid obesity and spermatogenic failure
Variation	info
Gene	CEP19
CLNDBN	Morbid obesity and spermatogenic failure
Reversed	0
HGVS	NC_000003.11:g.196434682G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000106311.2,