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rs1057524688

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524688(A;A)
Make rs1057524688(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position49374503
GeneKCNB1, LOC105372649
is asnp
is mentioned by
dbSNPrs1057524688
dbSNP (classic)rs1057524688
ClinGenrs1057524688
ebirs1057524688
HLIrs1057524688
Exacrs1057524688
Gnomadrs1057524688
Varsomers1057524688
LitVarrs1057524688
Maprs1057524688
PheGenIrs1057524688
Biobankrs1057524688
1000 genomesrs1057524688
hgdprs1057524688
ensemblrs1057524688
geneviewrs1057524688
scholarrs1057524688
googlers1057524688
pharmgkbrs1057524688
gwascentralrs1057524688
openSNPrs1057524688
23andMers1057524688
23andMe allrs1057524688
SNPshotrs1057524688
SNPdbers1057524688
MSV3drs1057524688
GWAS Ctlgrs1057524688
Max Magnitude0
ClinVar
Risk rs1057524688(A;A)
Alt rs1057524688(A;A)
Reference Rs1057524688(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNB1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.47991040C>T
CLNSRC
CLNACC RCV000441478.1,