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rs727503863

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503863(A;A)
Make rs727503863(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position60822121
GeneCHD7
is asnp
is mentioned by
dbSNPrs727503863
ebirs727503863
HLIrs727503863
Exacrs727503863
Varsomers727503863
Maprs727503863
PheGenIrs727503863
hapmaprs727503863
1000 genomesrs727503863
hgdprs727503863
ensemblrs727503863
gopubmedrs727503863
geneviewrs727503863
scholarrs727503863
googlers727503863
pharmgkbrs727503863
gwascentralrs727503863
openSNPrs727503863
23andMers727503863
23andMe allrs727503863
SNP Nexus

SNPshotrs727503863
SNPdbers727503863
MSV3drs727503863
GWAS Ctlgrs727503863
Max Magnitude0
ClinVar
Risk rs727503863(A;A)
Alt rs727503863(A;A)
Reference rs727503863(G;G)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61734680G>A
CLNSRC
CLNACC RCV000153009.3,