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rs1064793664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome8
Position60865457
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793664
dbSNP (classic)rs1064793664
ClinGenrs1064793664
ebirs1064793664
HLIrs1064793664
Exacrs1064793664
Gnomadrs1064793664
Varsomers1064793664
LitVarrs1064793664
Maprs1064793664
PheGenIrs1064793664
Biobankrs1064793664
1000 genomesrs1064793664
hgdprs1064793664
ensemblrs1064793664
geneviewrs1064793664
scholarrs1064793664
googlers1064793664
pharmgkbrs1064793664
gwascentralrs1064793664
openSNPrs1064793664
23andMers1064793664
23andMe allrs1064793664
SNPshotrs1064793664
SNPdbers1064793664
MSV3drs1064793664
GWAS Ctlgrs1064793664
Max Magnitude0
ClinVar
Risk rs1064793664(-;-)
Alt rs1064793664(-;-)
Reference Rs1064793664(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61778016delA
CLNSRC
CLNACC RCV000479418.1,