rs1057518489

Orientation

minus

Stabilized

minus

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

Make rs1057518489(A;G)

Make rs1057518489(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

63442446

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs1057518489
dbSNP (classic)	rs1057518489
ClinGen	rs1057518489
ebi	rs1057518489
HLI	rs1057518489
Exac	rs1057518489
Gnomad	rs1057518489
Varsome	rs1057518489
LitVar	rs1057518489
Map	rs1057518489
PheGenI	rs1057518489
Biobank	rs1057518489
1000 genomes	rs1057518489
hgdp	rs1057518489
ensembl	rs1057518489
geneview	rs1057518489
scholar	rs1057518489
google	rs1057518489
pharmgkb	rs1057518489
gwascentral	rs1057518489
openSNP	rs1057518489
23andMe	rs1057518489
SNPshot	rs1057518489
SNPdbe	rs1057518489
MSV3d	rs1057518489
GWAS Ctlg	rs1057518489

Max Magnitude

0

ClinVar
Risk	rs1057518489(G;G)
Alt	rs1057518489(G;G)
Reference	Rs1057518489(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62073799T>C
CLNSRC
CLNACC	RCV000412840.1,