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rs587777230

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777230(A;A)
Make rs587777230(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position196707811
GeneCEP19
is asnp
is mentioned by
dbSNPrs587777230
ebirs587777230
HLIrs587777230
Exacrs587777230
Varsomers587777230
Maprs587777230
PheGenIrs587777230
hapmaprs587777230
1000 genomesrs587777230
hgdprs587777230
ensemblrs587777230
gopubmedrs587777230
geneviewrs587777230
scholarrs587777230
googlers587777230
pharmgkbrs587777230
gwascentralrs587777230
openSNPrs587777230
23andMers587777230
23andMe allrs587777230
SNP Nexus

SNPshotrs587777230
SNPdbers587777230
MSV3drs587777230
GWAS Ctlgrs587777230
Max Magnitude0
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,