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rs387906885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906885(A;A)
Make rs387906885(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137101607
GeneMAN1B1
is asnp
is mentioned by
dbSNPrs387906885
ebirs387906885
HLIrs387906885
Exacrs387906885
Varsomers387906885
Maprs387906885
PheGenIrs387906885
hapmaprs387906885
1000 genomesrs387906885
hgdprs387906885
ensemblrs387906885
gopubmedrs387906885
geneviewrs387906885
scholarrs387906885
googlers387906885
pharmgkbrs387906885
gwascentralrs387906885
openSNPrs387906885
23andMers387906885
23andMe allrs387906885
SNP Nexus

SNPshotrs387906885
SNPdbers387906885
MSV3drs387906885
GWAS Ctlgrs387906885
Max Magnitude0
ClinVar
Risk rs387906885(A;A)
Alt rs387906885(A;A)
Reference rs387906885(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene MAN1B1
CLNDBN Mental retardation, autosomal recessive 15
Reversed 0
HGVS NC_000009.11:g.139996059G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023366.2,