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rs1064793769

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome8
Position60860924
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793769
dbSNP (old)rs1064793769
ClinGenrs1064793769
ebirs1064793769
HLIrs1064793769
Exacrs1064793769
Gnomadrs1064793769
Varsomers1064793769
Maprs1064793769
PheGenIrs1064793769
Biobankrs1064793769
1000 genomesrs1064793769
hgdprs1064793769
ensemblrs1064793769
gopubmedrs1064793769
geneviewrs1064793769
scholarrs1064793769
googlers1064793769
pharmgkbrs1064793769
gwascentralrs1064793769
openSNPrs1064793769
23andMers1064793769
23andMe allrs1064793769
SNP Nexus

SNPshotrs1064793769
SNPdbers1064793769
MSV3drs1064793769
GWAS Ctlgrs1064793769
Max Magnitude0
ClinVar
Risk rs1064793769(-;-)
Alt rs1064793769(-;-)
Reference Rs1064793769(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61773483delA
CLNSRC
CLNACC RCV000481551.1,