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rs1085307582

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position60801594
GeneCHD7
is asnp
is mentioned by
dbSNPrs1085307582
dbSNP (old)rs1085307582
ClinGenrs1085307582
ebirs1085307582
HLIrs1085307582
Exacrs1085307582
Gnomadrs1085307582
Varsomers1085307582
Maprs1085307582
PheGenIrs1085307582
Biobankrs1085307582
1000 genomesrs1085307582
hgdprs1085307582
ensemblrs1085307582
gopubmedrs1085307582
geneviewrs1085307582
scholarrs1085307582
googlers1085307582
pharmgkbrs1085307582
gwascentralrs1085307582
openSNPrs1085307582
23andMers1085307582
23andMe allrs1085307582
SNP Nexus

SNPshotrs1085307582
SNPdbers1085307582
MSV3drs1085307582
GWAS Ctlgrs1085307582
Max Magnitude0
ClinVar
Risk rs1085307582(T;T)
Alt rs1085307582(T;T)
Reference Rs1085307582(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61714153G>T
CLNSRC
CLNACC RCV000489857.1,