rs796052665

Orientation

minus

Stabilized

minus

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

Make rs796052665(AA;AA)

Make rs796052665(AA;GC)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63413478

Gene	KCNQ2, LOC105372724

is a	snp
is	mentioned by
dbSNP	rs796052665
dbSNP (classic)	rs796052665
ClinGen	rs796052665
ebi	rs796052665
HLI	rs796052665
Exac	rs796052665
Gnomad	rs796052665
Varsome	rs796052665
LitVar	rs796052665
Map	rs796052665
PheGenI	rs796052665
Biobank	rs796052665
1000 genomes	rs796052665
hgdp	rs796052665
ensembl	rs796052665
geneview	rs796052665
scholar	rs796052665
google	rs796052665
pharmgkb	rs796052665
gwascentral	rs796052665
openSNP	rs796052665
23andMe	rs796052665
SNPshot	rs796052665
SNPdbe	rs796052665
MSV3d	rs796052665
GWAS Ctlg	rs796052665

Max Magnitude

0

ClinVar
Risk	rs796052665(AA;AA)
Alt	rs796052665(AA;AA)
Reference	Rs796052665(GC;GC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.62044831_62044832delGCinsTT
CLNSRC
CLNACC	RCV000187944.1,