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rs1064793083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome8
Position60828682
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064793083
dbSNP (old)rs1064793083
ClinGenrs1064793083
ebirs1064793083
HLIrs1064793083
Exacrs1064793083
Gnomadrs1064793083
Varsomers1064793083
Maprs1064793083
PheGenIrs1064793083
Biobankrs1064793083
1000 genomesrs1064793083
hgdprs1064793083
ensemblrs1064793083
gopubmedrs1064793083
geneviewrs1064793083
scholarrs1064793083
googlers1064793083
pharmgkbrs1064793083
gwascentralrs1064793083
openSNPrs1064793083
23andMers1064793083
23andMe allrs1064793083
SNPshotrs1064793083
SNPdbers1064793083
MSV3drs1064793083
GWAS Ctlgrs1064793083
Max Magnitude0
ClinVar
Risk rs1064793083(T;T)
Alt rs1064793083(T;T)
Reference Rs1064793083(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61741241C>T
CLNSRC
CLNACC RCV000479619.1,