rs1057521887

Orientation

minus

Stabilized

minus

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

Make rs1057521887(A;G)

Make rs1057521887(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

49374622

Gene	KCNB1, LOC105372649

is a	snp
is	mentioned by
dbSNP	rs1057521887
dbSNP (classic)	rs1057521887
ClinGen	rs1057521887
ebi	rs1057521887
HLI	rs1057521887
Exac	rs1057521887
Gnomad	rs1057521887
Varsome	rs1057521887
LitVar	rs1057521887
Map	rs1057521887
PheGenI	rs1057521887
Biobank	rs1057521887
1000 genomes	rs1057521887
hgdp	rs1057521887
ensembl	rs1057521887
geneview	rs1057521887
scholar	rs1057521887
google	rs1057521887
pharmgkb	rs1057521887
gwascentral	rs1057521887
openSNP	rs1057521887
23andMe	rs1057521887
SNPshot	rs1057521887
SNPdbe	rs1057521887
MSV3d	rs1057521887
GWAS Ctlg	rs1057521887

Max Magnitude

0

ClinVar
Risk	rs1057521887(G;G)
Alt	rs1057521887(G;G)
Reference	Rs1057521887(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNB1
CLNDBN	not provided
Reversed	1
HGVS	NC_000020.10:g.47991159T>C
CLNSRC
CLNACC	RCV000417762.1,