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rs794727295

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CACTCCTCCTC;CACTCCTCCTC) 0 common in clinvar
Make rs794727295(-;-)
Make rs794727295(-;TCCTCCTCCAC)
Make rs794727295(TCCTCCTCCAC;TCCTCCTCCAC)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position60742656
GeneCHD7
is asnp
is mentioned by
dbSNPrs794727295
dbSNP (old)rs794727295
ClinGenrs794727295
ebirs794727295
HLIrs794727295
Exacrs794727295
Gnomadrs794727295
Varsomers794727295
Maprs794727295
PheGenIrs794727295
Biobankrs794727295
1000 genomesrs794727295
hgdprs794727295
ensemblrs794727295
gopubmedrs794727295
geneviewrs794727295
scholarrs794727295
googlers794727295
pharmgkbrs794727295
gwascentralrs794727295
openSNPrs794727295
23andMers794727295
23andMe allrs794727295
SNP Nexus

SNPshotrs794727295
SNPdbers794727295
MSV3drs794727295
GWAS Ctlgrs794727295
Max Magnitude0
ClinVar
Risk rs794727295(-;-)
Alt rs794727295(-;-)
Reference Rs794727295(CACTCCTCCTC;CACTCCTCCTC)
Significance Pathogenic
Disease CHARGE association
Variation info
Gene CHD7
CLNDBN CHARGE association
Reversed 0
HGVS NC_000008.10:g.61655215_61655225delTCCTCCTCCAC
CLNSRC
CLNACC RCV000175891.1,