rs1057521065

Orientation

minus

Stabilized

minus

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

Make rs1057521065(C;C)

Make rs1057521065(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

63968310

Gene

SCN4A

is a	snp
is	mentioned by
dbSNP	rs1057521065
dbSNP (classic)	rs1057521065
ClinGen	rs1057521065
ebi	rs1057521065
HLI	rs1057521065
Exac	rs1057521065
Gnomad	rs1057521065
Varsome	rs1057521065
LitVar	rs1057521065
Map	rs1057521065
PheGenI	rs1057521065
Biobank	rs1057521065
1000 genomes	rs1057521065
hgdp	rs1057521065
ensembl	rs1057521065
geneview	rs1057521065
scholar	rs1057521065
google	rs1057521065
pharmgkb	rs1057521065
gwascentral	rs1057521065
openSNP	rs1057521065
23andMe	rs1057521065
SNPshot	rs1057521065
SNPdbe	rs1057521065
MSV3d	rs1057521065
GWAS Ctlg	rs1057521065

Max Magnitude

0

ClinVar
Risk	rs1057521065(C;C)
Alt	rs1057521065(C;C)
Reference	Rs1057521065(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN4A
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.62045670A>G
CLNSRC
CLNACC	RCV000439261.1,