rs397514581

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs397514581(A;A)

Make rs397514581(A;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

63444711

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs397514581
dbSNP (classic)	rs397514581
ClinGen	rs397514581
ebi	rs397514581
HLI	rs397514581
Exac	rs397514581
Gnomad	rs397514581
Varsome	rs397514581
LitVar	rs397514581
Map	rs397514581
PheGenI	rs397514581
Biobank	rs397514581
1000 genomes	rs397514581
hgdp	rs397514581
ensembl	rs397514581
geneview	rs397514581
scholar	rs397514581
google	rs397514581
pharmgkb	rs397514581
gwascentral	rs397514581
openSNP	rs397514581
23andMe	rs397514581
SNPshot	rs397514581
SNPdbe	rs397514581
MSV3d	rs397514581
GWAS Ctlg	rs397514581

Max Magnitude

0

ClinVar
Risk	rs397514581(A;A)
Alt	rs397514581(A;A)
Reference	Rs397514581(G;G)
Significance	Other
Disease	Early infantile epileptic encephalopathy 7 not provided
Variation	info
Gene	KCNQ2
CLNDBN	Early infantile epileptic encephalopathy 7 not provided
Reversed	1
HGVS	NC_000020.10:g.62076064C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032979.5, RCV000187867.2,