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rs797045473

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045473(-;TG)
Make rs797045473(TG;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60862306
GeneCHD7
is asnp
is mentioned by
dbSNPrs797045473
ClinGenrs797045473
ebirs797045473
HLIrs797045473
Exacrs797045473
Varsomers797045473
Maprs797045473
PheGenIrs797045473
hapmaprs797045473
1000 genomesrs797045473
hgdprs797045473
ensemblrs797045473
gopubmedrs797045473
geneviewrs797045473
scholarrs797045473
googlers797045473
pharmgkbrs797045473
gwascentralrs797045473
openSNPrs797045473
23andMers797045473
23andMe allrs797045473
SNP Nexus

SNPshotrs797045473
SNPdbers797045473
MSV3drs797045473
GWAS Ctlgrs797045473
Max Magnitude0
ClinVar
Risk rs797045473(GT;GT)
Alt rs797045473(GT;GT)
Reference Rs797045473(-;-)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61774864_61774865dupTG
CLNSRC
CLNACC RCV000194957.1,