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rs1064797103

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome8
Position91078597
GeneOTUD6B
is asnp
is mentioned by
dbSNPrs1064797103
dbSNP (classic)rs1064797103
ClinGenrs1064797103
ebirs1064797103
HLIrs1064797103
Exacrs1064797103
Gnomadrs1064797103
Varsomers1064797103
LitVarrs1064797103
Maprs1064797103
PheGenIrs1064797103
Biobankrs1064797103
1000 genomesrs1064797103
hgdprs1064797103
ensemblrs1064797103
geneviewrs1064797103
scholarrs1064797103
googlers1064797103
pharmgkbrs1064797103
gwascentralrs1064797103
openSNPrs1064797103
23andMers1064797103
23andMe allrs1064797103
SNPshotrs1064797103
SNPdbers1064797103
MSV3drs1064797103
GWAS Ctlgrs1064797103
Max Magnitude0
ClinVar
Risk rs1064797103(G;G)
Alt rs1064797103(G;G)
Reference Rs1064797103(A;A)
Significance Pathogenic
Disease Intellectual developmental disorder with dysmorphic facies Dysmorphic features Intellectual disability Seizure Disorders
Variation info
Gene OTUD6B
CLNDBN Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies Dysmorphic features Intellectual disability Seizure Disorders
Reversed 0
HGVS NC_000008.10:g.92090825A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000487494.1, RCV000490986.1,