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rs1057520773

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520773(A;A)
Make rs1057520773(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63413527
GeneKCNQ2, LOC105372724
is asnp
is mentioned by
dbSNPrs1057520773
dbSNP (old)rs1057520773
ClinGenrs1057520773
ebirs1057520773
HLIrs1057520773
Exacrs1057520773
Gnomadrs1057520773
Varsomers1057520773
LitVarrs1057520773
Maprs1057520773
PheGenIrs1057520773
Biobankrs1057520773
1000 genomesrs1057520773
hgdprs1057520773
ensemblrs1057520773
gopubmedrs1057520773
geneviewrs1057520773
scholarrs1057520773
googlers1057520773
pharmgkbrs1057520773
gwascentralrs1057520773
openSNPrs1057520773
23andMers1057520773
23andMe allrs1057520773
SNPshotrs1057520773
SNPdbers1057520773
MSV3drs1057520773
GWAS Ctlgrs1057520773
Max Magnitude0
ClinVar
Risk rs1057520773(A;A)
Alt rs1057520773(A;A)
Reference Rs1057520773(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62044880G>T
CLNSRC
CLNACC RCV000439202.1,