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rs398124320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398124320(C;G)
Make rs398124320(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position60845380
GeneCHD7
is asnp
is mentioned by
dbSNPrs398124320
ebirs398124320
HLIrs398124320
Exacrs398124320
Varsomers398124320
Maprs398124320
PheGenIrs398124320
hapmaprs398124320
1000 genomesrs398124320
hgdprs398124320
ensemblrs398124320
gopubmedrs398124320
geneviewrs398124320
scholarrs398124320
googlers398124320
pharmgkbrs398124320
gwascentralrs398124320
openSNPrs398124320
23andMers398124320
23andMe allrs398124320
SNP Nexus

SNPshotrs398124320
SNPdbers398124320
MSV3drs398124320
GWAS Ctlgrs398124320
Max Magnitude0
ClinVar
Risk rs398124320(G,T;G,T)
Alt rs398124320(G,T;G,T)
Reference rs398124320(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61757939C>G
CLNSRC ClinVar Emory University
CLNACC RCV000081839.4,