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rs587776620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGT;AAGT) 0 common in clinvar
Make rs587776620(-;-)
Make rs587776620(-;AAGT)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position101729231
GeneCHPT1, SYCP3
is asnp
is mentioned by
dbSNPrs587776620
dbSNP (old)rs587776620
ClinGenrs587776620
ebirs587776620
HLIrs587776620
Exacrs587776620
Varsomers587776620
Maprs587776620
PheGenIrs587776620
Biobankrs587776620
1000 genomesrs587776620
hgdprs587776620
ensemblrs587776620
gopubmedrs587776620
geneviewrs587776620
scholarrs587776620
googlers587776620
pharmgkbrs587776620
gwascentralrs587776620
openSNPrs587776620
23andMers587776620
23andMe allrs587776620
SNP Nexus

SNPshotrs587776620
SNPdbers587776620
MSV3drs587776620
GWAS Ctlgrs587776620
Max Magnitude0
ClinVar
Risk rs587776620(-;-)
Alt rs587776620(-;-)
Reference Rs587776620(AAGT;AAGT)
Significance Pathogenic
Disease Spermatogenesis arrest
Variation info
Gene SYCP3 CHPT1
CLNDBN Spermatogenesis arrest
Reversed 0
HGVS NC_000012.11:g.102123009_102123012delAAGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000005703.3,