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rs1064793972

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position60856577
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793972
dbSNP (old)rs1064793972
ClinGenrs1064793972
ebirs1064793972
HLIrs1064793972
Exacrs1064793972
Gnomadrs1064793972
Varsomers1064793972
LitVarrs1064793972
Maprs1064793972
PheGenIrs1064793972
Biobankrs1064793972
1000 genomesrs1064793972
hgdprs1064793972
ensemblrs1064793972
gopubmedrs1064793972
geneviewrs1064793972
scholarrs1064793972
googlers1064793972
pharmgkbrs1064793972
gwascentralrs1064793972
openSNPrs1064793972
23andMers1064793972
23andMe allrs1064793972
SNPshotrs1064793972
SNPdbers1064793972
MSV3drs1064793972
GWAS Ctlgrs1064793972
Max Magnitude0
ClinVar
Risk rs1064793972(-;-)
Alt rs1064793972(-;-)
Reference Rs1064793972(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61769136delG
CLNSRC
CLNACC RCV000482952.1,