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rs1064793994

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position60742393
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793994
dbSNP (old)rs1064793994
ClinGenrs1064793994
ebirs1064793994
HLIrs1064793994
Exacrs1064793994
Gnomadrs1064793994
Varsomers1064793994
Maprs1064793994
PheGenIrs1064793994
Biobankrs1064793994
1000 genomesrs1064793994
hgdprs1064793994
ensemblrs1064793994
gopubmedrs1064793994
geneviewrs1064793994
scholarrs1064793994
googlers1064793994
pharmgkbrs1064793994
gwascentralrs1064793994
openSNPrs1064793994
23andMers1064793994
23andMe allrs1064793994
SNP Nexus

SNPshotrs1064793994
SNPdbers1064793994
MSV3drs1064793994
GWAS Ctlgrs1064793994
Max Magnitude0
ClinVar
Risk rs1064793994(T;T)
Alt rs1064793994(T;T)
Reference Rs1064793994(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61654952G>T
CLNSRC
CLNACC RCV000486665.1,