rs71352737

Orientation

plus

Stabilized

plus

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

Make rs71352737(A;A)

Make rs71352737(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

19

Position

49182889

Gene

TRPM4

is a	snp
is	mentioned by
dbSNP	rs71352737
dbSNP (classic)	rs71352737
ClinGen	rs71352737
ebi	rs71352737
HLI	rs71352737
Exac	rs71352737
Gnomad	rs71352737
Varsome	rs71352737
LitVar	rs71352737
Map	rs71352737
PheGenI	rs71352737
Biobank	rs71352737
1000 genomes	rs71352737
hgdp	rs71352737
ensembl	rs71352737
geneview	rs71352737
scholar	rs71352737
google	rs71352737
pharmgkb	rs71352737
gwascentral	rs71352737
openSNP	rs71352737
23andMe	rs71352737
SNPshot	rs71352737
SNPdbe	rs71352737
MSV3d	rs71352737
GWAS Ctlg	rs71352737

Max Magnitude

0

ClinVar
Risk	rs71352737(A;A)
Alt	rs71352737(A;A)
Reference	Rs71352737(G;G)
Significance	Probable-Pathogenic
Disease	Progressive familial heart block type 1B Sudden cardiac death not specified
Variation	info
Gene	TRPM4
CLNDBN	Progressive familial heart block type 1B Sudden cardiac death not specified
Reversed	0
HGVS	NC_000019.9:g.49686146G>A
CLNSRC
CLNACC	RCV000227821.1, RCV000256482.1, RCV000426179.1,