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rs1064796615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position60852964
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064796615
dbSNP (classic)rs1064796615
ClinGenrs1064796615
ebirs1064796615
HLIrs1064796615
Exacrs1064796615
Gnomadrs1064796615
Varsomers1064796615
LitVarrs1064796615
Maprs1064796615
PheGenIrs1064796615
Biobankrs1064796615
1000 genomesrs1064796615
hgdprs1064796615
ensemblrs1064796615
geneviewrs1064796615
scholarrs1064796615
googlers1064796615
pharmgkbrs1064796615
gwascentralrs1064796615
openSNPrs1064796615
23andMers1064796615
23andMe allrs1064796615
SNPshotrs1064796615
SNPdbers1064796615
MSV3drs1064796615
GWAS Ctlgrs1064796615
Max Magnitude0
ClinVar
Risk rs1064796615(C;C)
Alt rs1064796615(C;C)
Reference Rs1064796615(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61765523T>C
CLNSRC
CLNACC RCV000479492.1,