rs766751878

Orientation

plus

Stabilized

plus

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

Make rs766751878(C;C)

Make rs766751878(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

38550632

Gene

SCN5A

is a	snp
is	mentioned by
dbSNP	rs766751878
dbSNP (classic)	rs766751878
ClinGen	rs766751878
ebi	rs766751878
HLI	rs766751878
Exac	rs766751878
Gnomad	rs766751878
Varsome	rs766751878
LitVar	rs766751878
Map	rs766751878
PheGenI	rs766751878
Biobank	rs766751878
1000 genomes	rs766751878
hgdp	rs766751878
ensembl	rs766751878
geneview	rs766751878
scholar	rs766751878
google	rs766751878
pharmgkb	rs766751878
gwascentral	rs766751878
openSNP	rs766751878
23andMe	rs766751878
SNPshot	rs766751878
SNPdbe	rs766751878
MSV3d	rs766751878
GWAS Ctlg	rs766751878

Max Magnitude

0

ClinVar
Risk	rs766751878(C;C)
Alt	rs766751878(C;C)
Reference	Rs766751878(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN5A
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.38592123T>C
CLNSRC
CLNACC	RCV000183132.1,