rs778820577

Orientation

plus

Stabilized

plus

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

Make rs778820577(C;T)

Make rs778820577(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

63945392

Gene

SCN4A

is a	snp
is	mentioned by
dbSNP	rs778820577
dbSNP (classic)	rs778820577
ClinGen	rs778820577
ebi	rs778820577
HLI	rs778820577
Exac	rs778820577
Gnomad	rs778820577
Varsome	rs778820577
LitVar	rs778820577
Map	rs778820577
PheGenI	rs778820577
Biobank	rs778820577
1000 genomes	rs778820577
hgdp	rs778820577
ensembl	rs778820577
geneview	rs778820577
scholar	rs778820577
google	rs778820577
pharmgkb	rs778820577
gwascentral	rs778820577
openSNP	rs778820577
23andMe	rs778820577
SNPshot	rs778820577
SNPdbe	rs778820577
MSV3d	rs778820577
GWAS Ctlg	rs778820577

Max Magnitude

0

ClinVar
Risk	rs778820577(T;T)
Alt	rs778820577(T;T)
Reference	Rs778820577(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN4A
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.62022752C>T
CLNSRC
CLNACC	RCV000418825.1,