rs766755499

Orientation

plus

Stabilized

plus

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

Make rs766755499(C;C)

Make rs766755499(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63407326

Gene

KCNQ2

is a	snp
is	mentioned by
dbSNP	rs766755499
dbSNP (classic)	rs766755499
ClinGen	rs766755499
ebi	rs766755499
HLI	rs766755499
Exac	rs766755499
Gnomad	rs766755499
Varsome	rs766755499
LitVar	rs766755499
Map	rs766755499
PheGenI	rs766755499
Biobank	rs766755499
1000 genomes	rs766755499
hgdp	rs766755499
ensembl	rs766755499
geneview	rs766755499
scholar	rs766755499
google	rs766755499
pharmgkb	rs766755499
gwascentral	rs766755499
openSNP	rs766755499
23andMe	rs766755499
SNPshot	rs766755499
SNPdbe	rs766755499
MSV3d	rs766755499
GWAS Ctlg	rs766755499

Max Magnitude

0

ClinVar
Risk	rs766755499(C;C)
Alt	rs766755499(C;C)
Reference	Rs766755499(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	0
HGVS	NC_000020.10:g.62038679T>C
CLNSRC
CLNACC	RCV000187927.2,