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rs774225566

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs774225566(C;C)
Make rs774225566(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position133558953
GeneSYCE1
is asnp
is mentioned by
dbSNPrs774225566
ebirs774225566
HLIrs774225566
Exacrs774225566
Varsomers774225566
Maprs774225566
PheGenIrs774225566
hapmaprs774225566
1000 genomesrs774225566
hgdprs774225566
ensemblrs774225566
gopubmedrs774225566
geneviewrs774225566
scholarrs774225566
googlers774225566
pharmgkbrs774225566
gwascentralrs774225566
openSNPrs774225566
23andMers774225566
23andMe allrs774225566
SNP Nexus

SNPshotrs774225566
SNPdbers774225566
MSV3drs774225566
GWAS Ctlgrs774225566
Max Magnitude0
ClinVar
Risk rs774225566(C;C)
Alt rs774225566(C;C)
Reference rs774225566(T;T)
Significance Pathogenic
Disease Spermatogenic failure 15
Variation info
Gene SYCE1
CLNDBN Spermatogenic failure 15
Reversed 0
HGVS NC_000010.10:g.135372457T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000211704.2,