Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057520592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520592(A;A)
Make rs1057520592(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position92955513
GeneCHD2
is asnp
is mentioned by
dbSNPrs1057520592
dbSNP (old)rs1057520592
ClinGenrs1057520592
ebirs1057520592
HLIrs1057520592
Exacrs1057520592
Gnomadrs1057520592
Varsomers1057520592
Maprs1057520592
PheGenIrs1057520592
Biobankrs1057520592
1000 genomesrs1057520592
hgdprs1057520592
ensemblrs1057520592
gopubmedrs1057520592
geneviewrs1057520592
scholarrs1057520592
googlers1057520592
pharmgkbrs1057520592
gwascentralrs1057520592
openSNPrs1057520592
23andMers1057520592
23andMe allrs1057520592
SNPshotrs1057520592
SNPdbers1057520592
MSV3drs1057520592
GWAS Ctlgrs1057520592
Max Magnitude0
ClinVar
Risk rs1057520592(A;A)
Alt rs1057520592(A;A)
Reference Rs1057520592(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.93498743G>A
CLNSRC
CLNACC RCV000426945.1,