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rs1057519228

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519228(A;A)
Make rs1057519228(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position92953573
GeneCHD2
is asnp
is mentioned by
dbSNPrs1057519228
dbSNP (old)rs1057519228
ClinGenrs1057519228
ebirs1057519228
HLIrs1057519228
Exacrs1057519228
Gnomadrs1057519228
Varsomers1057519228
LitVarrs1057519228
Maprs1057519228
PheGenIrs1057519228
Biobankrs1057519228
1000 genomesrs1057519228
hgdprs1057519228
ensemblrs1057519228
gopubmedrs1057519228
geneviewrs1057519228
scholarrs1057519228
googlers1057519228
pharmgkbrs1057519228
gwascentralrs1057519228
openSNPrs1057519228
23andMers1057519228
23andMe allrs1057519228
SNPshotrs1057519228
SNPdbers1057519228
MSV3drs1057519228
GWAS Ctlgrs1057519228
Max Magnitude0
ClinVar
Risk rs1057519228(A;A)
Alt rs1057519228(A;A)
Reference Rs1057519228(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.93496803G>A
CLNSRC
CLNACC RCV000415729.1,