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rs1064797102

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome8
Position91071136
GeneOTUD6B, OTUD6B-AS1
is asnp
is mentioned by
dbSNPrs1064797102
dbSNP (old)rs1064797102
ClinGenrs1064797102
ebirs1064797102
HLIrs1064797102
Exacrs1064797102
Gnomadrs1064797102
Varsomers1064797102
Maprs1064797102
PheGenIrs1064797102
Biobankrs1064797102
1000 genomesrs1064797102
hgdprs1064797102
ensemblrs1064797102
gopubmedrs1064797102
geneviewrs1064797102
scholarrs1064797102
googlers1064797102
pharmgkbrs1064797102
gwascentralrs1064797102
openSNPrs1064797102
23andMers1064797102
23andMe allrs1064797102
SNPshotrs1064797102
SNPdbers1064797102
MSV3drs1064797102
GWAS Ctlgrs1064797102
Max Magnitude0
ClinVar
Risk rs1064797102(G;G)
Alt rs1064797102(G;G)
Reference Rs1064797102(A;A)
Significance Pathogenic
Disease Intellectual developmental disorder with dysmorphic facies Dysmorphic features Intellectual disability Seizure Disorders
Variation info
Gene LOC100506365 OTUD6B-AS1 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.92083364A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000488135.1, RCV000491932.1,