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rs1057517919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517919(A;A)
Make rs1057517919(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63413534
GeneKCNQ2, LOC105372724
is asnp
is mentioned by
dbSNPrs1057517919
dbSNP (old)rs1057517919
ClinGenrs1057517919
ebirs1057517919
HLIrs1057517919
Exacrs1057517919
Gnomadrs1057517919
Varsomers1057517919
Maprs1057517919
PheGenIrs1057517919
Biobankrs1057517919
1000 genomesrs1057517919
hgdprs1057517919
ensemblrs1057517919
gopubmedrs1057517919
geneviewrs1057517919
scholarrs1057517919
googlers1057517919
pharmgkbrs1057517919
gwascentralrs1057517919
openSNPrs1057517919
23andMers1057517919
23andMe allrs1057517919
SNPshotrs1057517919
SNPdbers1057517919
MSV3drs1057517919
GWAS Ctlgrs1057517919
Max Magnitude0
ClinVar
Risk rs1057517919(A;A)
Alt rs1057517919(A;A)
Reference Rs1057517919(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62044887C>T
CLNSRC
CLNACC RCV000413758.1,