rs886039396

Orientation

minus

Stabilized

minus

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

Make rs886039396(C;T)

Make rs886039396(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

20

Position

49374626

Gene	KCNB1, LOC105372649

is a	snp
is	mentioned by
dbSNP	rs886039396
dbSNP (classic)	rs886039396
ClinGen	rs886039396
ebi	rs886039396
HLI	rs886039396
Exac	rs886039396
Gnomad	rs886039396
Varsome	rs886039396
LitVar	rs886039396
Map	rs886039396
PheGenI	rs886039396
Biobank	rs886039396
1000 genomes	rs886039396
hgdp	rs886039396
ensembl	rs886039396
geneview	rs886039396
scholar	rs886039396
google	rs886039396
pharmgkb	rs886039396
gwascentral	rs886039396
openSNP	rs886039396
23andMe	rs886039396
SNPshot	rs886039396
SNPdbe	rs886039396
MSV3d	rs886039396
GWAS Ctlg	rs886039396

Max Magnitude

0

ClinVar
Risk	rs886039396(T;T)
Alt	rs886039396(T;T)
Reference	Rs886039396(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNB1
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.47991163G>A
CLNSRC
CLNACC	RCV000255550.1,