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rs1057520734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520734(C;T)
Make rs1057520734(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60742555
GeneCHD7
is asnp
is mentioned by
dbSNPrs1057520734
dbSNP (old)rs1057520734
ClinGenrs1057520734
ebirs1057520734
HLIrs1057520734
Exacrs1057520734
Varsomers1057520734
Maprs1057520734
PheGenIrs1057520734
Biobankrs1057520734
1000 genomesrs1057520734
hgdprs1057520734
ensemblrs1057520734
gopubmedrs1057520734
geneviewrs1057520734
scholarrs1057520734
googlers1057520734
pharmgkbrs1057520734
gwascentralrs1057520734
openSNPrs1057520734
23andMers1057520734
23andMe allrs1057520734
SNP Nexus

SNPshotrs1057520734
SNPdbers1057520734
MSV3drs1057520734
GWAS Ctlgrs1057520734
Max Magnitude0
ClinVar
Risk rs1057520734(T;T)
Alt rs1057520734(T;T)
Reference Rs1057520734(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61655114C>T
CLNSRC
CLNACC RCV000441742.1,