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rs864622523

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864622523(A;C)
Make rs864622523(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60828661
GeneCHD7
is asnp
is mentioned by
dbSNPrs864622523
ebirs864622523
HLIrs864622523
Exacrs864622523
Varsomers864622523
Maprs864622523
PheGenIrs864622523
hapmaprs864622523
1000 genomesrs864622523
hgdprs864622523
ensemblrs864622523
gopubmedrs864622523
geneviewrs864622523
scholarrs864622523
googlers864622523
pharmgkbrs864622523
gwascentralrs864622523
openSNPrs864622523
23andMers864622523
23andMe allrs864622523
SNP Nexus

SNPshotrs864622523
SNPdbers864622523
MSV3drs864622523
GWAS Ctlgrs864622523
Max Magnitude0
ClinVar
Risk rs864622523(C;C)
Alt rs864622523(C;C)
Reference rs864622523(A;A)
Significance Probable-Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61741220A>C
CLNSRC
CLNACC RCV000205203.1,