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rs1057517957

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517957(-;C)
Make rs1057517957(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position60860950
GeneCHD7
is asnp
is mentioned by
dbSNPrs1057517957
dbSNP (old)rs1057517957
ClinGenrs1057517957
ebirs1057517957
HLIrs1057517957
Exacrs1057517957
Gnomadrs1057517957
Varsomers1057517957
Maprs1057517957
PheGenIrs1057517957
Biobankrs1057517957
1000 genomesrs1057517957
hgdprs1057517957
ensemblrs1057517957
gopubmedrs1057517957
geneviewrs1057517957
scholarrs1057517957
googlers1057517957
pharmgkbrs1057517957
gwascentralrs1057517957
openSNPrs1057517957
23andMers1057517957
23andMe allrs1057517957
SNP Nexus

SNPshotrs1057517957
SNPdbers1057517957
MSV3drs1057517957
GWAS Ctlgrs1057517957
Max Magnitude0
ClinVar
Risk rs1057517957(C;C)
Alt rs1057517957(C;C)
Reference Rs1057517957(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61773509dupC
CLNSRC
CLNACC RCV000413712.1,