Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057521077

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521077(C;C)
Make rs1057521077(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60822604
GeneCHD7
is asnp
is mentioned by
dbSNPrs1057521077
dbSNP (old)rs1057521077
ClinGenrs1057521077
ebirs1057521077
HLIrs1057521077
Exacrs1057521077
Gnomadrs1057521077
Varsomers1057521077
Maprs1057521077
PheGenIrs1057521077
Biobankrs1057521077
1000 genomesrs1057521077
hgdprs1057521077
ensemblrs1057521077
gopubmedrs1057521077
geneviewrs1057521077
scholarrs1057521077
googlers1057521077
pharmgkbrs1057521077
gwascentralrs1057521077
openSNPrs1057521077
23andMers1057521077
23andMe allrs1057521077
SNP Nexus

SNPshotrs1057521077
SNPdbers1057521077
MSV3drs1057521077
GWAS Ctlgrs1057521077
Max Magnitude0
ClinVar
Risk rs1057521077(C;C)
Alt rs1057521077(C;C)
Reference Rs1057521077(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61735163T>C
CLNSRC
CLNACC RCV000445135.1,