rs1057524860

Orientation

minus

Stabilized

minus

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

Make rs1057524860(A;G)

Make rs1057524860(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

63438692

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs1057524860
dbSNP (classic)	rs1057524860
ClinGen	rs1057524860
ebi	rs1057524860
HLI	rs1057524860
Exac	rs1057524860
Gnomad	rs1057524860
Varsome	rs1057524860
LitVar	rs1057524860
Map	rs1057524860
PheGenI	rs1057524860
Biobank	rs1057524860
1000 genomes	rs1057524860
hgdp	rs1057524860
ensembl	rs1057524860
geneview	rs1057524860
scholar	rs1057524860
google	rs1057524860
pharmgkb	rs1057524860
gwascentral	rs1057524860
openSNP	rs1057524860
23andMe	rs1057524860
SNPshot	rs1057524860
SNPdbe	rs1057524860
MSV3d	rs1057524860
GWAS Ctlg	rs1057524860

Max Magnitude

0

ClinVar
Risk	rs1057524860(G;G)
Alt	rs1057524860(G;G)
Reference	Rs1057524860(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62070045T>C
CLNSRC
CLNACC	RCV000437292.1,