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rs1057524677

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524677(C;T)
Make rs1057524677(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position21426154
GeneCHD8
is asnp
is mentioned by
dbSNPrs1057524677
dbSNP (old)rs1057524677
ClinGenrs1057524677
ebirs1057524677
HLIrs1057524677
Exacrs1057524677
Gnomadrs1057524677
Varsomers1057524677
Maprs1057524677
PheGenIrs1057524677
Biobankrs1057524677
1000 genomesrs1057524677
hgdprs1057524677
ensemblrs1057524677
gopubmedrs1057524677
geneviewrs1057524677
scholarrs1057524677
googlers1057524677
pharmgkbrs1057524677
gwascentralrs1057524677
openSNPrs1057524677
23andMers1057524677
23andMe allrs1057524677
SNPshotrs1057524677
SNPdbers1057524677
MSV3drs1057524677
GWAS Ctlgrs1057524677
Max Magnitude0
ClinVar
Risk rs1057524677(T;T)
Alt rs1057524677(T;T)
Reference Rs1057524677(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21894313G>A
CLNSRC
CLNACC RCV000440969.1,