rs1057520773

Orientation

minus

Stabilized

minus

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

Make rs1057520773(A;A)

Make rs1057520773(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

63413527

Gene	KCNQ2, LOC105372724

is a	snp
is	mentioned by
dbSNP	rs1057520773
dbSNP (classic)	rs1057520773
ClinGen	rs1057520773
ebi	rs1057520773
HLI	rs1057520773
Exac	rs1057520773
Gnomad	rs1057520773
Varsome	rs1057520773
LitVar	rs1057520773
Map	rs1057520773
PheGenI	rs1057520773
Biobank	rs1057520773
1000 genomes	rs1057520773
hgdp	rs1057520773
ensembl	rs1057520773
geneview	rs1057520773
scholar	rs1057520773
google	rs1057520773
pharmgkb	rs1057520773
gwascentral	rs1057520773
openSNP	rs1057520773
23andMe	rs1057520773
SNPshot	rs1057520773
SNPdbe	rs1057520773
MSV3d	rs1057520773
GWAS Ctlg	rs1057520773

Max Magnitude

0

ClinVar
Risk	rs1057520773(A;A)
Alt	rs1057520773(A;A)
Reference	Rs1057520773(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62044880G>T
CLNSRC
CLNACC	RCV000439202.1,