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rs1057523712

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523712(C;C)
Make rs1057523712(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position21402055
GeneCHD8
is asnp
is mentioned by
dbSNPrs1057523712
dbSNP (classic)rs1057523712
ClinGenrs1057523712
ebirs1057523712
HLIrs1057523712
Exacrs1057523712
Gnomadrs1057523712
Varsomers1057523712
LitVarrs1057523712
Maprs1057523712
PheGenIrs1057523712
Biobankrs1057523712
1000 genomesrs1057523712
hgdprs1057523712
ensemblrs1057523712
geneviewrs1057523712
scholarrs1057523712
googlers1057523712
pharmgkbrs1057523712
gwascentralrs1057523712
openSNPrs1057523712
23andMers1057523712
23andMe allrs1057523712
SNPshotrs1057523712
SNPdbers1057523712
MSV3drs1057523712
GWAS Ctlgrs1057523712
Max Magnitude0
ClinVar
Risk rs1057523712(C;C)
Alt rs1057523712(C;C)
Reference Rs1057523712(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21870214C>G
CLNSRC
CLNACC RCV000432820.1,