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rs797044919

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044919(-;C)
Make rs797044919(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60845365
GeneCHD7
is asnp
is mentioned by
dbSNPrs797044919
ClinGenrs797044919
ebirs797044919
HLIrs797044919
Exacrs797044919
Varsomers797044919
Maprs797044919
PheGenIrs797044919
hapmaprs797044919
1000 genomesrs797044919
hgdprs797044919
ensemblrs797044919
gopubmedrs797044919
geneviewrs797044919
scholarrs797044919
googlers797044919
pharmgkbrs797044919
gwascentralrs797044919
openSNPrs797044919
23andMers797044919
23andMe allrs797044919
SNP Nexus

SNPshotrs797044919
SNPdbers797044919
MSV3drs797044919
GWAS Ctlgrs797044919
Max Magnitude0
ClinVar
Risk rs797044919(C;C)
Alt rs797044919(C;C)
Reference Rs797044919(;)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CHD7
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000008.10:g.61757924dupC
CLNSRC
CLNACC RCV000190754.1,