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rs199981784

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199981784(C;T)
Make rs199981784(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60850475
GeneCHD7
is asnp
is mentioned by
dbSNPrs199981784
dbSNP (old)rs199981784
ClinGenrs199981784
ebirs199981784
HLIrs199981784
Exacrs199981784
Gnomadrs199981784
Varsomers199981784
Maprs199981784
PheGenIrs199981784
Biobankrs199981784
1000 genomesrs199981784
hgdprs199981784
ensemblrs199981784
gopubmedrs199981784
geneviewrs199981784
scholarrs199981784
googlers199981784
pharmgkbrs199981784
gwascentralrs199981784
openSNPrs199981784
23andMers199981784
23andMe allrs199981784
SNPshotrs199981784
SNPdbers199981784
MSV3drs199981784
GWAS Ctlgrs199981784
Max Magnitude0
ClinVar
Risk rs199981784(T;T)
Alt rs199981784(T;T)
Reference Rs199981784(C;C)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61763034C>A
CLNSRC
CLNACC RCV000492724.1,