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rs869312849

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312849(A;C)
Make rs869312849(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position505182
GeneCSNK2A1
is asnp
is mentioned by
dbSNPrs869312849
ebirs869312849
HLIrs869312849
Exacrs869312849
Varsomers869312849
Maprs869312849
PheGenIrs869312849
hapmaprs869312849
1000 genomesrs869312849
hgdprs869312849
ensemblrs869312849
gopubmedrs869312849
geneviewrs869312849
scholarrs869312849
googlers869312849
pharmgkbrs869312849
gwascentralrs869312849
openSNPrs869312849
23andMers869312849
23andMe allrs869312849
SNP Nexus

SNPshotrs869312849
SNPdbers869312849
MSV3drs869312849
GWAS Ctlgrs869312849
Max Magnitude0
ClinVar
Risk rs869312849(C;C)
Alt rs869312849(C;C)
Reference rs869312849(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.485826T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210375.1, RCV000239568.1,