Have questions? Visit https://www.reddit.com/r/SNPedia

rs398124322

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124322(C;C)
Make rs398124322(C;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position60852497
GeneCHD7
is asnp
is mentioned by
dbSNPrs398124322
ebirs398124322
HLIrs398124322
Exacrs398124322
Varsomers398124322
Maprs398124322
PheGenIrs398124322
hapmaprs398124322
1000 genomesrs398124322
hgdprs398124322
ensemblrs398124322
gopubmedrs398124322
geneviewrs398124322
scholarrs398124322
googlers398124322
pharmgkbrs398124322
gwascentralrs398124322
openSNPrs398124322
23andMers398124322
23andMe allrs398124322
SNP Nexus

SNPshotrs398124322
SNPdbers398124322
MSV3drs398124322
GWAS Ctlgrs398124322
Max Magnitude0
ClinVar
Risk rs398124322(C;C)
Alt rs398124322(C;C)
Reference rs398124322(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61765056G>C
CLNSRC ClinVar
CLNACC RCV000081843.4,