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rs730882197

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882197(-;-)
Make rs730882197(-;ACAA)
Make rs730882197(ACAA;ACAA)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position4525342
GeneC12orf4
is asnp
is mentioned by
dbSNPrs730882197
ebirs730882197
HLIrs730882197
Exacrs730882197
Varsomers730882197
Maprs730882197
PheGenIrs730882197
hapmaprs730882197
1000 genomesrs730882197
hgdprs730882197
ensemblrs730882197
gopubmedrs730882197
geneviewrs730882197
scholarrs730882197
googlers730882197
pharmgkbrs730882197
gwascentralrs730882197
openSNPrs730882197
23andMers730882197
23andMe allrs730882197
SNP Nexus

SNPshotrs730882197
SNPdbers730882197
MSV3drs730882197
GWAS Ctlgrs730882197
Max Magnitude0
ClinVar
Risk rs730882197(ACAA;ACAA)
Alt rs730882197(ACAA;ACAA)
Reference rs730882197(;)
Significance Probable-Pathogenic
Disease Attention deficit hyperactivity disorder Intellectual disability Muscular hypotonia
Variation info
Gene C12orf4
CLNDBN Attention deficit hyperactivity disorder Intellectual disability Muscular hypotonia
Reversed 1
HGVS NC_000012.11:g.4634508_4634509insTTGT
CLNSRC
CLNACC RCV000162098.1,