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rs1085307830

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position60781131
GeneCHD7
is asnp
is mentioned by
dbSNPrs1085307830
dbSNP (old)rs1085307830
ClinGenrs1085307830
ebirs1085307830
HLIrs1085307830
Exacrs1085307830
Gnomadrs1085307830
Varsomers1085307830
Maprs1085307830
PheGenIrs1085307830
Biobankrs1085307830
1000 genomesrs1085307830
hgdprs1085307830
ensemblrs1085307830
gopubmedrs1085307830
geneviewrs1085307830
scholarrs1085307830
googlers1085307830
pharmgkbrs1085307830
gwascentralrs1085307830
openSNPrs1085307830
23andMers1085307830
23andMe allrs1085307830
SNPshotrs1085307830
SNPdbers1085307830
MSV3drs1085307830
GWAS Ctlgrs1085307830
Max Magnitude0
ClinVar
Risk rs1085307830(-;-)
Alt rs1085307830(-;-)
Reference Rs1085307830(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD7
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.61693690delG
CLNSRC
CLNACC RCV000489678.1,