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rs1064793432

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Chromosome8
Position60801534
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793432
dbSNP (old)rs1064793432
ClinGenrs1064793432
ebirs1064793432
HLIrs1064793432
Exacrs1064793432
Gnomadrs1064793432
Varsomers1064793432
Maprs1064793432
PheGenIrs1064793432
Biobankrs1064793432
1000 genomesrs1064793432
hgdprs1064793432
ensemblrs1064793432
gopubmedrs1064793432
geneviewrs1064793432
scholarrs1064793432
googlers1064793432
pharmgkbrs1064793432
gwascentralrs1064793432
openSNPrs1064793432
23andMers1064793432
23andMe allrs1064793432
SNPshotrs1064793432
SNPdbers1064793432
MSV3drs1064793432
GWAS Ctlgrs1064793432
Max Magnitude0
ClinVar
Risk rs1064793432(-;-)
Alt rs1064793432(-;-)
Reference Rs1064793432(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61714093_61714094delGT
CLNSRC
CLNACC RCV000482114.1,