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rs1057518621

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518621(A;A)
Make rs1057518621(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position49374652
GeneKCNB1, LOC105372649
is asnp
is mentioned by
dbSNPrs1057518621
dbSNP (old)rs1057518621
ClinGenrs1057518621
ebirs1057518621
HLIrs1057518621
Exacrs1057518621
Gnomadrs1057518621
Varsomers1057518621
Maprs1057518621
PheGenIrs1057518621
Biobankrs1057518621
1000 genomesrs1057518621
hgdprs1057518621
ensemblrs1057518621
gopubmedrs1057518621
geneviewrs1057518621
scholarrs1057518621
googlers1057518621
pharmgkbrs1057518621
gwascentralrs1057518621
openSNPrs1057518621
23andMers1057518621
23andMe allrs1057518621
SNPshotrs1057518621
SNPdbers1057518621
MSV3drs1057518621
GWAS Ctlgrs1057518621
Max Magnitude0
ClinVar
Risk rs1057518621(A;A)
Alt rs1057518621(A;A)
Reference Rs1057518621(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNB1
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.47991189C>T
CLNSRC
CLNACC RCV000413312.1,