Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064793996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Chromosome8
Position60742393
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793996
dbSNP (old)rs1064793996
ClinGenrs1064793996
ebirs1064793996
HLIrs1064793996
Exacrs1064793996
Varsomers1064793996
Maprs1064793996
PheGenIrs1064793996
Biobankrs1064793996
1000 genomesrs1064793996
hgdprs1064793996
ensemblrs1064793996
gopubmedrs1064793996
geneviewrs1064793996
scholarrs1064793996
googlers1064793996
pharmgkbrs1064793996
gwascentralrs1064793996
openSNPrs1064793996
23andMers1064793996
23andMe allrs1064793996
SNP Nexus

SNPshotrs1064793996
SNPdbers1064793996
MSV3drs1064793996
GWAS Ctlgrs1064793996
Max Magnitude0
ClinVar
Risk rs1064793996(TA;TA)
Alt rs1064793996(TA;TA)
Reference Rs1064793996(GG;GG)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61654952_61654953delGGinsTA
CLNSRC
CLNACC RCV000484055.1,