rs1057521989

Orientation

minus

Stabilized

minus

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

Make rs1057521989(A;T)

Make rs1057521989(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

45461944

Gene

HCN1

is a	snp
is	mentioned by
dbSNP	rs1057521989
dbSNP (classic)	rs1057521989
ClinGen	rs1057521989
ebi	rs1057521989
HLI	rs1057521989
Exac	rs1057521989
Gnomad	rs1057521989
Varsome	rs1057521989
LitVar	rs1057521989
Map	rs1057521989
PheGenI	rs1057521989
Biobank	rs1057521989
1000 genomes	rs1057521989
hgdp	rs1057521989
ensembl	rs1057521989
geneview	rs1057521989
scholar	rs1057521989
google	rs1057521989
pharmgkb	rs1057521989
gwascentral	rs1057521989
openSNP	rs1057521989
23andMe	rs1057521989
SNPshot	rs1057521989
SNPdbe	rs1057521989
MSV3d	rs1057521989
GWAS Ctlg	rs1057521989

Max Magnitude

0

ClinVar
Risk	rs1057521989(T;T)
Alt	rs1057521989(T;T)
Reference	Rs1057521989(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HCN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000005.9:g.45462046T>A
CLNSRC
CLNACC	RCV000444585.1,