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rs1064793463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position60836101
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793463
dbSNP (old)rs1064793463
ClinGenrs1064793463
ebirs1064793463
HLIrs1064793463
Exacrs1064793463
Gnomadrs1064793463
Varsomers1064793463
Maprs1064793463
PheGenIrs1064793463
Biobankrs1064793463
1000 genomesrs1064793463
hgdprs1064793463
ensemblrs1064793463
gopubmedrs1064793463
geneviewrs1064793463
scholarrs1064793463
googlers1064793463
pharmgkbrs1064793463
gwascentralrs1064793463
openSNPrs1064793463
23andMers1064793463
23andMe allrs1064793463
SNPshotrs1064793463
SNPdbers1064793463
MSV3drs1064793463
GWAS Ctlgrs1064793463
Max Magnitude0
ClinVar
Risk rs1064793463(-;-)
Alt rs1064793463(-;-)
Reference Rs1064793463(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61748660delT
CLNSRC
CLNACC RCV000484664.1,