rs199722402

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs199722402(C;T)

Make rs199722402(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

40987186

Gene

INO80

is a	snp
is	mentioned by
dbSNP	rs199722402
dbSNP (classic)	rs199722402
ClinGen	rs199722402
ebi	rs199722402
HLI	rs199722402
Exac	rs199722402
Gnomad	rs199722402
Varsome	rs199722402
LitVar	rs199722402
Map	rs199722402
PheGenI	rs199722402
Biobank	rs199722402
1000 genomes	rs199722402
hgdp	rs199722402
ensembl	rs199722402
geneview	rs199722402
scholar	rs199722402
google	rs199722402
pharmgkb	rs199722402
gwascentral	rs199722402
openSNP	rs199722402
23andMe	rs199722402
SNPshot	rs199722402
SNPdbe	rs199722402
MSV3d	rs199722402
GWAS Ctlg	rs199722402

Max Magnitude

0

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,