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rs398124321

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124321(A;A)
Make rs398124321(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position60850486
GeneCHD7
is asnp
is mentioned by
dbSNPrs398124321
ebirs398124321
HLIrs398124321
Exacrs398124321
Varsomers398124321
Maprs398124321
PheGenIrs398124321
hapmaprs398124321
1000 genomesrs398124321
hgdprs398124321
ensemblrs398124321
gopubmedrs398124321
geneviewrs398124321
scholarrs398124321
googlers398124321
pharmgkbrs398124321
gwascentralrs398124321
openSNPrs398124321
23andMers398124321
23andMe allrs398124321
SNP Nexus

SNPshotrs398124321
SNPdbers398124321
MSV3drs398124321
GWAS Ctlgrs398124321
Max Magnitude0
ClinVar
Risk rs398124321(A,T;A,T)
Alt rs398124321(A,T;A,T)
Reference rs398124321(G;G)
Significance Pathogenic
Disease not provided CHARGE association
Variation info
Gene CHD7
CLNDBN not provided CHARGE association
Reversed 0
HGVS NC_000008.10:g.61763045G>A
CLNSRC HGMD
CLNACC RCV000081841.3, RCV000176678.1,