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rs1085307905

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome20
Position63472177
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1085307905
dbSNP (old)rs1085307905
ClinGenrs1085307905
ebirs1085307905
HLIrs1085307905
Exacrs1085307905
Gnomadrs1085307905
Varsomers1085307905
Maprs1085307905
PheGenIrs1085307905
Biobankrs1085307905
1000 genomesrs1085307905
hgdprs1085307905
ensemblrs1085307905
gopubmedrs1085307905
geneviewrs1085307905
scholarrs1085307905
googlers1085307905
pharmgkbrs1085307905
gwascentralrs1085307905
openSNPrs1085307905
23andMers1085307905
23andMe allrs1085307905
SNPshotrs1085307905
SNPdbers1085307905
MSV3drs1085307905
GWAS Ctlgrs1085307905
Max Magnitude0
ClinVar
Risk rs1085307905(C;C)
Alt rs1085307905(C;C)
Reference Rs1085307905(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62103531dup
CLNSRC
CLNACC RCV000490208.1,