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rs797044912

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044912(C;T)
Make rs797044912(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position93020140
GeneCHD2
is asnp
is mentioned by
dbSNPrs797044912
ebirs797044912
HLIrs797044912
Exacrs797044912
Varsomers797044912
Maprs797044912
PheGenIrs797044912
hapmaprs797044912
1000 genomesrs797044912
hgdprs797044912
ensemblrs797044912
gopubmedrs797044912
geneviewrs797044912
scholarrs797044912
googlers797044912
pharmgkbrs797044912
gwascentralrs797044912
openSNPrs797044912
23andMers797044912
23andMe allrs797044912
SNP Nexus

SNPshotrs797044912
SNPdbers797044912
MSV3drs797044912
GWAS Ctlgrs797044912
Max Magnitude0
ClinVar
Risk rs797044912(T;T)
Alt rs797044912(T;T)
Reference rs797044912(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CHD2
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000015.9:g.93563370C>T
CLNSRC
CLNACC RCV000190741.1,