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rs1057517713

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517713(A;A)
Make rs1057517713(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60849065
GeneCHD7
is asnp
is mentioned by
dbSNPrs1057517713
dbSNP (old)rs1057517713
ClinGenrs1057517713
ebirs1057517713
HLIrs1057517713
Exacrs1057517713
Gnomadrs1057517713
Varsomers1057517713
LitVarrs1057517713
Maprs1057517713
PheGenIrs1057517713
Biobankrs1057517713
1000 genomesrs1057517713
hgdprs1057517713
ensemblrs1057517713
gopubmedrs1057517713
geneviewrs1057517713
scholarrs1057517713
googlers1057517713
pharmgkbrs1057517713
gwascentralrs1057517713
openSNPrs1057517713
23andMers1057517713
23andMe allrs1057517713
SNPshotrs1057517713
SNPdbers1057517713
MSV3drs1057517713
GWAS Ctlgrs1057517713
Max Magnitude0
ClinVar
Risk rs1057517713(A;A)
Alt rs1057517713(A;A)
Reference Rs1057517713(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61761624G>A
CLNSRC
CLNACC RCV000413976.1,