rs1057518492

Orientation

minus

Stabilized

minus

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

Make rs1057518492(A;A)

Make rs1057518492(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

63414088

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs1057518492
dbSNP (classic)	rs1057518492
ClinGen	rs1057518492
ebi	rs1057518492
HLI	rs1057518492
Exac	rs1057518492
Gnomad	rs1057518492
Varsome	rs1057518492
LitVar	rs1057518492
Map	rs1057518492
PheGenI	rs1057518492
Biobank	rs1057518492
1000 genomes	rs1057518492
hgdp	rs1057518492
ensembl	rs1057518492
geneview	rs1057518492
scholar	rs1057518492
google	rs1057518492
pharmgkb	rs1057518492
gwascentral	rs1057518492
openSNP	rs1057518492
23andMe	rs1057518492
SNPshot	rs1057518492
SNPdbe	rs1057518492
MSV3d	rs1057518492
GWAS Ctlg	rs1057518492

Max Magnitude

0

ClinVar
Risk	rs1057518492(A;A)
Alt	rs1057518492(A;A)
Reference	Rs1057518492(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62045441C>T
CLNSRC
CLNACC	RCV000412766.1,