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rs28937885

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28937885(A;A)
Make rs28937885(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position138945951
GeneC3orf72, FOXL2
is asnp
is mentioned by
dbSNPrs28937885
ebirs28937885
HLIrs28937885
Exacrs28937885
Varsomers28937885
Maprs28937885
PheGenIrs28937885
hapmaprs28937885
1000 genomesrs28937885
hgdprs28937885
ensemblrs28937885
gopubmedrs28937885
geneviewrs28937885
scholarrs28937885
googlers28937885
pharmgkbrs28937885
gwascentralrs28937885
openSNPrs28937885
23andMers28937885
23andMe allrs28937885
SNP Nexus

SNPshotrs28937885
SNPdbers28937885
MSV3drs28937885
GWAS Ctlgrs28937885
Max Magnitude0
OMIM605597
DescPREMATURE OVARIAN FAILURE 3
Variant0017
Relatedalso
Neighborrs28937884
Distance521


ClinVar
Risk rs28937885(A;A)
Alt rs28937885(A;A)
Reference rs28937885(T;T)
Significance Pathogenic
Disease Premature ovarian failure 3
Variation info
Gene FOXL2 FOXL2NB C3orf72 LINC01391
CLNDBN Premature ovarian failure 3
Reversed 1
HGVS NC_000003.11:g.138664793A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005145.2,



[PMID 17277738OA-icon.png] FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.