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rs797045472

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045472(-;C)
Make rs797045472(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60854412
GeneCHD7
is asnp
is mentioned by
dbSNPrs797045472
ClinGenrs797045472
ebirs797045472
HLIrs797045472
Exacrs797045472
Varsomers797045472
Maprs797045472
PheGenIrs797045472
hapmaprs797045472
1000 genomesrs797045472
hgdprs797045472
ensemblrs797045472
gopubmedrs797045472
geneviewrs797045472
scholarrs797045472
googlers797045472
pharmgkbrs797045472
gwascentralrs797045472
openSNPrs797045472
23andMers797045472
23andMe allrs797045472
SNP Nexus

SNPshotrs797045472
SNPdbers797045472
MSV3drs797045472
GWAS Ctlgrs797045472
Max Magnitude0
ClinVar
Risk rs797045472(C;C)
Alt rs797045472(C;C)
Reference Rs797045472(;)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61766971dupC
CLNSRC
CLNACC RCV000193258.1,