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rs797044725

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044725(-;ACCCTCTGTCA)
Make rs797044725(ACCCTCTGTCA;ACCCTCTGTCA)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60865402
GeneCHD7
is asnp
is mentioned by
dbSNPrs797044725
ClinGenrs797044725
ebirs797044725
HLIrs797044725
Exacrs797044725
Varsomers797044725
Maprs797044725
PheGenIrs797044725
hapmaprs797044725
1000 genomesrs797044725
hgdprs797044725
ensemblrs797044725
gopubmedrs797044725
geneviewrs797044725
scholarrs797044725
googlers797044725
pharmgkbrs797044725
gwascentralrs797044725
openSNPrs797044725
23andMers797044725
23andMe allrs797044725
SNP Nexus

SNPshotrs797044725
SNPdbers797044725
MSV3drs797044725
GWAS Ctlgrs797044725
Max Magnitude0
ClinVar
Risk rs797044725(AACCCTCTGTC;AACCCTCTGTC)
Alt rs797044725(AACCCTCTGTC;AACCCTCTGTC)
Reference Rs797044725(;)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61777951_61777961dupACCCTCTGTCA
CLNSRC
CLNACC RCV000177948.1,