rs1057517919

Orientation

minus

Stabilized

minus

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

Make rs1057517919(A;A)

Make rs1057517919(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

63413534

Gene	KCNQ2, LOC105372724

is a	snp
is	mentioned by
dbSNP	rs1057517919
dbSNP (classic)	rs1057517919
ClinGen	rs1057517919
ebi	rs1057517919
HLI	rs1057517919
Exac	rs1057517919
Gnomad	rs1057517919
Varsome	rs1057517919
LitVar	rs1057517919
Map	rs1057517919
PheGenI	rs1057517919
Biobank	rs1057517919
1000 genomes	rs1057517919
hgdp	rs1057517919
ensembl	rs1057517919
geneview	rs1057517919
scholar	rs1057517919
google	rs1057517919
pharmgkb	rs1057517919
gwascentral	rs1057517919
openSNP	rs1057517919
23andMe	rs1057517919
SNPshot	rs1057517919
SNPdbe	rs1057517919
MSV3d	rs1057517919
GWAS Ctlg	rs1057517919

Max Magnitude

0

ClinVar
Risk	rs1057517919(A;A)
Alt	rs1057517919(A;A)
Reference	Rs1057517919(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62044887C>T
CLNSRC
CLNACC	RCV000413758.1,