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rs1057521078

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521078(A;G)
Make rs1057521078(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60841989
GeneCHD7
is asnp
is mentioned by
dbSNPrs1057521078
dbSNP (old)rs1057521078
ClinGenrs1057521078
ebirs1057521078
HLIrs1057521078
Exacrs1057521078
Gnomadrs1057521078
Varsomers1057521078
Maprs1057521078
PheGenIrs1057521078
Biobankrs1057521078
1000 genomesrs1057521078
hgdprs1057521078
ensemblrs1057521078
gopubmedrs1057521078
geneviewrs1057521078
scholarrs1057521078
googlers1057521078
pharmgkbrs1057521078
gwascentralrs1057521078
openSNPrs1057521078
23andMers1057521078
23andMe allrs1057521078
SNP Nexus

SNPshotrs1057521078
SNPdbers1057521078
MSV3drs1057521078
GWAS Ctlgrs1057521078
Max Magnitude0
ClinVar
Risk rs1057521078(G;G)
Alt rs1057521078(G;G)
Reference Rs1057521078(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61754548A>G
CLNSRC
CLNACC RCV000426210.1,