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rs875989885

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989885(C;T)
Make rs875989885(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position133555706
GeneSYCE1
is asnp
is mentioned by
dbSNPrs875989885
ebirs875989885
HLIrs875989885
Exacrs875989885
Varsomers875989885
Maprs875989885
PheGenIrs875989885
hapmaprs875989885
1000 genomesrs875989885
hgdprs875989885
ensemblrs875989885
gopubmedrs875989885
geneviewrs875989885
scholarrs875989885
googlers875989885
pharmgkbrs875989885
gwascentralrs875989885
openSNPrs875989885
23andMers875989885
23andMe allrs875989885
SNP Nexus

SNPshotrs875989885
SNPdbers875989885
MSV3drs875989885
GWAS Ctlgrs875989885
Max Magnitude0
ClinVar
Risk rs875989885(T;T)
Alt rs875989885(T;T)
Reference rs875989885(C;C)
Significance Pathogenic
Disease Premature ovarian failure 12
Variation info
Gene SYCE1
CLNDBN Premature ovarian failure 12
Reversed 1
HGVS NC_000010.10:g.135369210G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000211464.1,