rs199473292

Orientation

minus

Stabilized

minus

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

Make rs199473292(C;C)

Make rs199473292(C;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

38551391

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs199473292
dbSNP (classic)	rs199473292
ClinGen	rs199473292
ebi	rs199473292
HLI	rs199473292
Exac	rs199473292
Gnomad	rs199473292
Varsome	rs199473292
LitVar	rs199473292
Map	rs199473292
PheGenI	rs199473292
Biobank	rs199473292
1000 genomes	rs199473292
hgdp	rs199473292
ensembl	rs199473292
geneview	rs199473292
scholar	rs199473292
google	rs199473292
pharmgkb	rs199473292
gwascentral	rs199473292
openSNP	rs199473292
23andMe	rs199473292
SNPshot	rs199473292
SNPdbe	rs199473292
MSV3d	rs199473292
GWAS Ctlg	rs199473292

Max Magnitude

0

ClinVar
Risk	rs199473292(A;A) rs199473292(C;C)
Alt	rs199473292(A;A) rs199473292(C;C)
Reference	Rs199473292(G;G)
Significance	Untested
Disease	Brugada syndrome not specified
Variation	info
Gene	SCN5A
CLNDBN	Brugada syndrome not specified
Reversed	1
HGVS	NC_000003.11:g.38592882C>G; NC_000003.11:g.38592882C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058733.2, RCV000183094.2,