Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518236

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518236(C;T)
Make rs1057518236(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position92949036
GeneCHD2
is asnp
is mentioned by
dbSNPrs1057518236
dbSNP (old)rs1057518236
ClinGenrs1057518236
ebirs1057518236
HLIrs1057518236
Exacrs1057518236
Gnomadrs1057518236
Varsomers1057518236
Maprs1057518236
PheGenIrs1057518236
Biobankrs1057518236
1000 genomesrs1057518236
hgdprs1057518236
ensemblrs1057518236
gopubmedrs1057518236
geneviewrs1057518236
scholarrs1057518236
googlers1057518236
pharmgkbrs1057518236
gwascentralrs1057518236
openSNPrs1057518236
23andMers1057518236
23andMe allrs1057518236
SNPshotrs1057518236
SNPdbers1057518236
MSV3drs1057518236
GWAS Ctlgrs1057518236
Max Magnitude0
ClinVar
Risk rs1057518236(T;T)
Alt rs1057518236(T;T)
Reference Rs1057518236(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD2
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.93492266C>T
CLNSRC
CLNACC RCV000413801.1,