rs797044872

Orientation

minus

Stabilized

minus

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

Make rs797044872(A;A)

Make rs797044872(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

50323685

Gene

KCNC3

is a	snp
is	mentioned by
dbSNP	rs797044872
dbSNP (classic)	rs797044872
ClinGen	rs797044872
ebi	rs797044872
HLI	rs797044872
Exac	rs797044872
Gnomad	rs797044872
Varsome	rs797044872
LitVar	rs797044872
Map	rs797044872
PheGenI	rs797044872
Biobank	rs797044872
1000 genomes	rs797044872
hgdp	rs797044872
ensembl	rs797044872
geneview	rs797044872
scholar	rs797044872
google	rs797044872
pharmgkb	rs797044872
gwascentral	rs797044872
openSNP	rs797044872
23andMe	rs797044872
SNPshot	rs797044872
SNPdbe	rs797044872
MSV3d	rs797044872
GWAS Ctlg	rs797044872

Max Magnitude

0

ClinVar
Risk	rs797044872(A;A)
Alt	rs797044872(A;A)
Reference	Rs797044872(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases not provided
Variation	info
Gene	KCNC3
CLNDBN	Inborn genetic diseases not provided
Reversed	1
HGVS	NC_000019.9:g.50826942C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000190682.1, RCV000277864.1,