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rs1057518092

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518092(A;A)
Make rs1057518092(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position499909
GeneCSNK2A1
is asnp
is mentioned by
dbSNPrs1057518092
dbSNP (old)rs1057518092
ClinGenrs1057518092
ebirs1057518092
HLIrs1057518092
Exacrs1057518092
Gnomadrs1057518092
Varsomers1057518092
Maprs1057518092
PheGenIrs1057518092
Biobankrs1057518092
1000 genomesrs1057518092
hgdprs1057518092
ensemblrs1057518092
gopubmedrs1057518092
geneviewrs1057518092
scholarrs1057518092
googlers1057518092
pharmgkbrs1057518092
gwascentralrs1057518092
openSNPrs1057518092
23andMers1057518092
23andMe allrs1057518092
SNPshotrs1057518092
SNPdbers1057518092
MSV3drs1057518092
GWAS Ctlgrs1057518092
Max Magnitude0
ClinVar
Risk rs1057518092(A;A)
Alt rs1057518092(A;A)
Reference Rs1057518092(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CSNK2A1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.480553C>T
CLNSRC
CLNACC RCV000413359.1,