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rs1064795519

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome8
Position60823870
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064795519
dbSNP (old)rs1064795519
ClinGenrs1064795519
ebirs1064795519
HLIrs1064795519
Exacrs1064795519
Gnomadrs1064795519
Varsomers1064795519
Maprs1064795519
PheGenIrs1064795519
Biobankrs1064795519
1000 genomesrs1064795519
hgdprs1064795519
ensemblrs1064795519
gopubmedrs1064795519
geneviewrs1064795519
scholarrs1064795519
googlers1064795519
pharmgkbrs1064795519
gwascentralrs1064795519
openSNPrs1064795519
23andMers1064795519
23andMe allrs1064795519
SNPshotrs1064795519
SNPdbers1064795519
MSV3drs1064795519
GWAS Ctlgrs1064795519
Max Magnitude0
ClinVar
Risk rs1064795519(T;T)
Alt rs1064795519(T;T)
Reference Rs1064795519(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61736429C>T
CLNSRC
CLNACC RCV000480751.1,