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rs1057524339

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524339(A;G)
Make rs1057524339(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position21408557
GeneCHD8
is asnp
is mentioned by
dbSNPrs1057524339
dbSNP (old)rs1057524339
ClinGenrs1057524339
ebirs1057524339
HLIrs1057524339
Exacrs1057524339
Gnomadrs1057524339
Varsomers1057524339
Maprs1057524339
PheGenIrs1057524339
Biobankrs1057524339
1000 genomesrs1057524339
hgdprs1057524339
ensemblrs1057524339
gopubmedrs1057524339
geneviewrs1057524339
scholarrs1057524339
googlers1057524339
pharmgkbrs1057524339
gwascentralrs1057524339
openSNPrs1057524339
23andMers1057524339
23andMe allrs1057524339
SNPshotrs1057524339
SNPdbers1057524339
MSV3drs1057524339
GWAS Ctlgrs1057524339
Max Magnitude0
ClinVar
Risk rs1057524339(G;G)
Alt rs1057524339(G;G)
Reference Rs1057524339(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CHD8
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.21876716T>C
CLNSRC
CLNACC RCV000423157.1,