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rs1057521887

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521887(A;G)
Make rs1057521887(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position49374622
GeneKCNB1, LOC105372649
is asnp
is mentioned by
dbSNPrs1057521887
dbSNP (old)rs1057521887
ClinGenrs1057521887
ebirs1057521887
HLIrs1057521887
Exacrs1057521887
Gnomadrs1057521887
Varsomers1057521887
Maprs1057521887
PheGenIrs1057521887
Biobankrs1057521887
1000 genomesrs1057521887
hgdprs1057521887
ensemblrs1057521887
gopubmedrs1057521887
geneviewrs1057521887
scholarrs1057521887
googlers1057521887
pharmgkbrs1057521887
gwascentralrs1057521887
openSNPrs1057521887
23andMers1057521887
23andMe allrs1057521887
SNPshotrs1057521887
SNPdbers1057521887
MSV3drs1057521887
GWAS Ctlgrs1057521887
Max Magnitude0
ClinVar
Risk rs1057521887(G;G)
Alt rs1057521887(G;G)
Reference Rs1057521887(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNB1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.47991159T>C
CLNSRC
CLNACC RCV000417762.1,