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rs1057524708

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524708(G;T)
Make rs1057524708(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position497720
GeneCSNK2A1
is asnp
is mentioned by
dbSNPrs1057524708
dbSNP (old)rs1057524708
ClinGenrs1057524708
ebirs1057524708
HLIrs1057524708
Exacrs1057524708
Gnomadrs1057524708
Varsomers1057524708
Maprs1057524708
PheGenIrs1057524708
Biobankrs1057524708
1000 genomesrs1057524708
hgdprs1057524708
ensemblrs1057524708
gopubmedrs1057524708
geneviewrs1057524708
scholarrs1057524708
googlers1057524708
pharmgkbrs1057524708
gwascentralrs1057524708
openSNPrs1057524708
23andMers1057524708
23andMe allrs1057524708
SNPshotrs1057524708
SNPdbers1057524708
MSV3drs1057524708
GWAS Ctlgrs1057524708
Max Magnitude0
ClinVar
Risk rs1057524708(T;T)
Alt rs1057524708(T;T)
Reference Rs1057524708(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CSNK2A1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.478364C>A
CLNSRC
CLNACC RCV000431425.1,