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rs864309609

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864309609(C;C)
Make rs864309609(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60836175
GeneCHD7
is asnp
is mentioned by
dbSNPrs864309609
ebirs864309609
HLIrs864309609
Exacrs864309609
Varsomers864309609
Maprs864309609
PheGenIrs864309609
hapmaprs864309609
1000 genomesrs864309609
hgdprs864309609
ensemblrs864309609
gopubmedrs864309609
geneviewrs864309609
scholarrs864309609
googlers864309609
pharmgkbrs864309609
gwascentralrs864309609
openSNPrs864309609
23andMers864309609
23andMe allrs864309609
SNP Nexus

SNPshotrs864309609
SNPdbers864309609
MSV3drs864309609
GWAS Ctlgrs864309609
Max Magnitude0
ClinVar
Risk rs864309609(C;C)
Alt rs864309609(C;C)
Reference rs864309609(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61748734T>C
CLNSRC
CLNACC RCV000203151.1,