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rs1064796242

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome8
Position60836915
GeneCHD7
is asnp
is mentioned by
dbSNPrs1064796242
dbSNP (old)rs1064796242
ClinGenrs1064796242
ebirs1064796242
HLIrs1064796242
Exacrs1064796242
Gnomadrs1064796242
Varsomers1064796242
Maprs1064796242
PheGenIrs1064796242
Biobankrs1064796242
1000 genomesrs1064796242
hgdprs1064796242
ensemblrs1064796242
gopubmedrs1064796242
geneviewrs1064796242
scholarrs1064796242
googlers1064796242
pharmgkbrs1064796242
gwascentralrs1064796242
openSNPrs1064796242
23andMers1064796242
23andMe allrs1064796242
SNP Nexus

SNPshotrs1064796242
SNPdbers1064796242
MSV3drs1064796242
GWAS Ctlgrs1064796242
Max Magnitude0
ClinVar
Risk rs1064796242(A;A)
Alt rs1064796242(A;A)
Reference Rs1064796242(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61749474T>A
CLNSRC
CLNACC RCV000485513.1,