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

rs786204200

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204200(-;-)
Make rs786204200(-;A)
Make rs786204200(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60742920
GeneCHD7
is asnp
is mentioned by
dbSNPrs786204200
ebirs786204200
HLIrs786204200
Exacrs786204200
Varsomers786204200
Maprs786204200
PheGenIrs786204200
hapmaprs786204200
1000 genomesrs786204200
hgdprs786204200
ensemblrs786204200
gopubmedrs786204200
geneviewrs786204200
scholarrs786204200
googlers786204200
pharmgkbrs786204200
gwascentralrs786204200
openSNPrs786204200
23andMers786204200
23andMe allrs786204200
SNP Nexus

SNPshotrs786204200
SNPdbers786204200
MSV3drs786204200
GWAS Ctlgrs786204200
Max Magnitude0
ClinVar
Risk rs786204200(A;A)
Alt rs786204200(A;A)
Reference rs786204200(;)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61655479dupA
CLNSRC
CLNACC RCV000168287.1,