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rs869312840

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312840(A;G)
Make rs869312840(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position492282
GeneCSNK2A1
is asnp
is mentioned by
dbSNPrs869312840
ebirs869312840
HLIrs869312840
Exacrs869312840
Varsomers869312840
Maprs869312840
PheGenIrs869312840
hapmaprs869312840
1000 genomesrs869312840
hgdprs869312840
ensemblrs869312840
gopubmedrs869312840
geneviewrs869312840
scholarrs869312840
googlers869312840
pharmgkbrs869312840
gwascentralrs869312840
openSNPrs869312840
23andMers869312840
23andMe allrs869312840
SNP Nexus

SNPshotrs869312840
SNPdbers869312840
MSV3drs869312840
GWAS Ctlgrs869312840
Max Magnitude0
ClinVar
Risk rs869312840(G;G)
Alt rs869312840(G;G)
Reference rs869312840(A;A)
Significance Pathogenic
Disease not provided Okur-chung neurodevelopmental syndrome
Variation info
Gene CSNK2A1
CLNDBN not provided Okur-chung neurodevelopmental syndrome
Reversed 1
HGVS NC_000020.10:g.472926T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000210367.1, RCV000239482.1,