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rs1064796449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome15
Position93012388
GeneCHD2
is asnp
is mentioned by
dbSNPrs1064796449
dbSNP (old)rs1064796449
ClinGenrs1064796449
ebirs1064796449
HLIrs1064796449
Exacrs1064796449
Gnomadrs1064796449
Varsomers1064796449
Maprs1064796449
PheGenIrs1064796449
Biobankrs1064796449
1000 genomesrs1064796449
hgdprs1064796449
ensemblrs1064796449
gopubmedrs1064796449
geneviewrs1064796449
scholarrs1064796449
googlers1064796449
pharmgkbrs1064796449
gwascentralrs1064796449
openSNPrs1064796449
23andMers1064796449
23andMe allrs1064796449
SNPshotrs1064796449
SNPdbers1064796449
MSV3drs1064796449
GWAS Ctlgrs1064796449
Max Magnitude0
ClinVar
Risk rs1064796449(T;T)
Alt rs1064796449(T;T)
Reference Rs1064796449(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.93555618C>T
CLNSRC
CLNACC RCV000484816.1,