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rs587777703

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAGGCA;CAGGCA) 0 common in clinvar
Make rs587777703(CAGGCA;T)
Make rs587777703(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position87335448
GeneFBXO31
is asnp
is mentioned by
dbSNPrs587777703
ebirs587777703
HLIrs587777703
Exacrs587777703
Varsomers587777703
Maprs587777703
PheGenIrs587777703
hapmaprs587777703
1000 genomesrs587777703
hgdprs587777703
ensemblrs587777703
gopubmedrs587777703
geneviewrs587777703
scholarrs587777703
googlers587777703
pharmgkbrs587777703
gwascentralrs587777703
openSNPrs587777703
23andMers587777703
23andMe allrs587777703
SNP Nexus

SNPshotrs587777703
SNPdbers587777703
MSV3drs587777703
GWAS Ctlgrs587777703
Max Magnitude0
ClinVar
Risk rs587777703(T;T)
Alt rs587777703(T;T)
Reference rs587777703(CAGGCA;CAGGCA)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene FBXO31
CLNDBN Mental retardation, autosomal recessive 45
Reversed 0
HGVS NC_000016.9:g.87369054_87369059delCAGGCAinsT
CLNSRC OMIM Allelic Variant
CLNACC RCV000144039.2,