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rs199722402

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199722402(C;T)
Make rs199722402(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position40987186
GeneINO80
is asnp
is mentioned by
dbSNPrs199722402
ebirs199722402
HLIrs199722402
Exacrs199722402
Varsomers199722402
Maprs199722402
PheGenIrs199722402
hapmaprs199722402
1000 genomesrs199722402
hgdprs199722402
ensemblrs199722402
gopubmedrs199722402
geneviewrs199722402
scholarrs199722402
googlers199722402
pharmgkbrs199722402
gwascentralrs199722402
openSNPrs199722402
23andMers199722402
23andMe allrs199722402
SNP Nexus

SNPshotrs199722402
SNPdbers199722402
MSV3drs199722402
GWAS Ctlgrs199722402
Max Magnitude0
ClinVar
Risk rs199722402(T;T)
Alt rs199722402(T;T)
Reference rs199722402(C;C)
Significance Probable-Pathogenic
Disease Intellectual disability Primary microcephaly Seizures
Variation info
Gene INO80
CLNDBN Intellectual disability Primary microcephaly Seizures
Reversed 0
HGVS NC_000015.9:g.41279384C>T
CLNSRC
CLNACC RCV000162143.1,