rs772800738

Orientation

plus

Stabilized

plus

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

Make rs772800738(C;C)

Make rs772800738(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

20

Position

63433878

Gene	KCNQ2, LOC105372721

is a	snp
is	mentioned by
dbSNP	rs772800738
dbSNP (classic)	rs772800738
ClinGen	rs772800738
ebi	rs772800738
HLI	rs772800738
Exac	rs772800738
Gnomad	rs772800738
Varsome	rs772800738
LitVar	rs772800738
Map	rs772800738
PheGenI	rs772800738
Biobank	rs772800738
1000 genomes	rs772800738
hgdp	rs772800738
ensembl	rs772800738
geneview	rs772800738
scholar	rs772800738
google	rs772800738
pharmgkb	rs772800738
gwascentral	rs772800738
openSNP	rs772800738
23andMe	rs772800738
SNPshot	rs772800738
SNPdbe	rs772800738
MSV3d	rs772800738
GWAS Ctlg	rs772800738

Max Magnitude

0

ClinVar
Risk	rs772800738(A;A) rs772800738(C;C)
Alt	rs772800738(A;A) rs772800738(C;C)
Reference	Rs772800738(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ2
CLNDBN	not provided
Reversed	0
HGVS	NC_000020.10:g.62065231T>A
CLNSRC
CLNACC	RCV000187894.1,