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rs863223399

From SNPedia

Orientationminus
Make rs863223399(-;-)
Make rs863223399(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position47176198
GeneIER3IP1
is asnp
is mentioned by
dbSNPrs863223399
ClinGenrs863223399
ebirs863223399
HLIrs863223399
Exacrs863223399
Varsomers863223399
Maprs863223399
PheGenIrs863223399
hapmaprs863223399
1000 genomesrs863223399
hgdprs863223399
ensemblrs863223399
gopubmedrs863223399
geneviewrs863223399
scholarrs863223399
googlers863223399
pharmgkbrs863223399
gwascentralrs863223399
openSNPrs863223399
23andMers863223399
23andMe allrs863223399
SNP Nexus

SNPshotrs863223399
SNPdbers863223399
MSV3drs863223399
GWAS Ctlgrs863223399
Max Magnitude
ClinVar
Risk
Alt
Reference Rs863223399(T;T)
Significance Pathogenic
Disease Microcephaly
Variation info
Gene IER3IP1
CLNDBN Microcephaly, epilepsy, and diabetes syndrome
Reversed 1
HGVS NC_000018.9:g.44702569delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000190474.2,