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rs769825641

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs769825641(A;G)
Make rs769825641(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position101729109
GeneCHPT1, LOC101928981, SYCP3
is asnp
is mentioned by
dbSNPrs769825641
ebirs769825641
HLIrs769825641
Exacrs769825641
Varsomers769825641
Maprs769825641
PheGenIrs769825641
hapmaprs769825641
1000 genomesrs769825641
hgdprs769825641
ensemblrs769825641
gopubmedrs769825641
geneviewrs769825641
scholarrs769825641
googlers769825641
pharmgkbrs769825641
gwascentralrs769825641
openSNPrs769825641
23andMers769825641
23andMe allrs769825641
SNP Nexus

SNPshotrs769825641
SNPdbers769825641
MSV3drs769825641
GWAS Ctlgrs769825641
Max Magnitude0
ClinVar
Risk rs769825641(G;G)
Alt rs769825641(G;G)
Reference rs769825641(A;A)
Significance Pathogenic
Disease Spermatogenesis arrest
Variation info
Gene SYCP3 CHPT1
CLNDBN Spermatogenesis arrest
Reversed 0
HGVS NC_000012.11:g.102122887A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005704.3,