rs1057523728

Orientation

minus

Stabilized

minus

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

Make rs1057523728(A;A)

Make rs1057523728(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

63439692

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs1057523728
dbSNP (classic)	rs1057523728
ClinGen	rs1057523728
ebi	rs1057523728
HLI	rs1057523728
Exac	rs1057523728
Gnomad	rs1057523728
Varsome	rs1057523728
LitVar	rs1057523728
Map	rs1057523728
PheGenI	rs1057523728
Biobank	rs1057523728
1000 genomes	rs1057523728
hgdp	rs1057523728
ensembl	rs1057523728
geneview	rs1057523728
scholar	rs1057523728
google	rs1057523728
pharmgkb	rs1057523728
gwascentral	rs1057523728
openSNP	rs1057523728
23andMe	rs1057523728
SNPshot	rs1057523728
SNPdbe	rs1057523728
MSV3d	rs1057523728
GWAS Ctlg	rs1057523728

Max Magnitude

0

ClinVar
Risk	rs1057523728(A;A)
Alt	rs1057523728(A;A)
Reference	Rs1057523728(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62071045A>G; NC_000020.10:g.62071045A>T
CLNSRC
CLNACC	RCV000494098.1, RCV000437231.1,