rs1057524599

Orientation

minus

Stabilized

minus

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

Make rs1057524599(A;G)

Make rs1057524599(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

63444718

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs1057524599
dbSNP (classic)	rs1057524599
ClinGen	rs1057524599
ebi	rs1057524599
HLI	rs1057524599
Exac	rs1057524599
Gnomad	rs1057524599
Varsome	rs1057524599
LitVar	rs1057524599
Map	rs1057524599
PheGenI	rs1057524599
Biobank	rs1057524599
1000 genomes	rs1057524599
hgdp	rs1057524599
ensembl	rs1057524599
geneview	rs1057524599
scholar	rs1057524599
google	rs1057524599
pharmgkb	rs1057524599
gwascentral	rs1057524599
openSNP	rs1057524599
23andMe	rs1057524599
SNPshot	rs1057524599
SNPdbe	rs1057524599
MSV3d	rs1057524599
GWAS Ctlg	rs1057524599

Max Magnitude

0

ClinVar
Risk	rs1057524599(G;G)
Alt	rs1057524599(G;G)
Reference	Rs1057524599(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62076071T>C
CLNSRC
CLNACC	RCV000434548.1,