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rs1064793084

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position60838255
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793084
dbSNP (old)rs1064793084
ClinGenrs1064793084
ebirs1064793084
HLIrs1064793084
Exacrs1064793084
Varsomers1064793084
Maprs1064793084
PheGenIrs1064793084
Biobankrs1064793084
1000 genomesrs1064793084
hgdprs1064793084
ensemblrs1064793084
gopubmedrs1064793084
geneviewrs1064793084
scholarrs1064793084
googlers1064793084
pharmgkbrs1064793084
gwascentralrs1064793084
openSNPrs1064793084
23andMers1064793084
23andMe allrs1064793084
SNP Nexus

SNPshotrs1064793084
SNPdbers1064793084
MSV3drs1064793084
GWAS Ctlgrs1064793084
Max Magnitude0
ClinVar
Risk rs1064793084(A;A)
Alt rs1064793084(A;A)
Reference Rs1064793084(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61750814G>A
CLNSRC
CLNACC RCV000483704.1,