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rs797045461

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045461(-;G)
Make rs797045461(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60781012
GeneCHD7
is asnp
is mentioned by
dbSNPrs797045461
ClinGenrs797045461
ebirs797045461
HLIrs797045461
Exacrs797045461
Varsomers797045461
Maprs797045461
PheGenIrs797045461
hapmaprs797045461
1000 genomesrs797045461
hgdprs797045461
ensemblrs797045461
gopubmedrs797045461
geneviewrs797045461
scholarrs797045461
googlers797045461
pharmgkbrs797045461
gwascentralrs797045461
openSNPrs797045461
23andMers797045461
23andMe allrs797045461
SNP Nexus

SNPshotrs797045461
SNPdbers797045461
MSV3drs797045461
GWAS Ctlgrs797045461
Max Magnitude0
ClinVar
Risk rs797045461(G;G)
Alt rs797045461(G;G)
Reference Rs797045461(;)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61693571dupG
CLNSRC
CLNACC RCV000194479.1,