rs1057518068

Orientation

minus

Stabilized

minus

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

Make rs1057518068(C;C)

Make rs1057518068(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

63442479

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs1057518068
dbSNP (classic)	rs1057518068
ClinGen	rs1057518068
ebi	rs1057518068
HLI	rs1057518068
Exac	rs1057518068
Gnomad	rs1057518068
Varsome	rs1057518068
LitVar	rs1057518068
Map	rs1057518068
PheGenI	rs1057518068
Biobank	rs1057518068
1000 genomes	rs1057518068
hgdp	rs1057518068
ensembl	rs1057518068
geneview	rs1057518068
scholar	rs1057518068
google	rs1057518068
pharmgkb	rs1057518068
gwascentral	rs1057518068
openSNP	rs1057518068
23andMe	rs1057518068
SNPshot	rs1057518068
SNPdbe	rs1057518068
MSV3d	rs1057518068
GWAS Ctlg	rs1057518068

Max Magnitude

0

ClinVar
Risk	rs1057518068(C;C)
Alt	rs1057518068(C;C)
Reference	Rs1057518068(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62073832A>G
CLNSRC
CLNACC	RCV000414529.1,