rs1057519124

Orientation

minus

Stabilized

minus

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

Make rs1057519124(A;A)

Make rs1057519124(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

63442405

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs1057519124
dbSNP (classic)	rs1057519124
ClinGen	rs1057519124
ebi	rs1057519124
HLI	rs1057519124
Exac	rs1057519124
Gnomad	rs1057519124
Varsome	rs1057519124
LitVar	rs1057519124
Map	rs1057519124
PheGenI	rs1057519124
Biobank	rs1057519124
1000 genomes	rs1057519124
hgdp	rs1057519124
ensembl	rs1057519124
geneview	rs1057519124
scholar	rs1057519124
google	rs1057519124
pharmgkb	rs1057519124
gwascentral	rs1057519124
openSNP	rs1057519124
23andMe	rs1057519124
SNPshot	rs1057519124
SNPdbe	rs1057519124
MSV3d	rs1057519124
GWAS Ctlg	rs1057519124

Max Magnitude

0

ClinVar
Risk	rs1057519124(A;A)
Alt	rs1057519124(A;A)
Reference	Rs1057519124(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62073758C>T
CLNSRC
CLNACC	RCV000416126.1,