rs373150395

Orientation

plus

Stabilized

plus

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

Make rs373150395(C;T)

Make rs373150395(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

63948003

Gene

SCN4A

is a	snp
is	mentioned by
dbSNP	rs373150395
dbSNP (classic)	rs373150395
ClinGen	rs373150395
ebi	rs373150395
HLI	rs373150395
Exac	rs373150395
Gnomad	rs373150395
Varsome	rs373150395
LitVar	rs373150395
Map	rs373150395
PheGenI	rs373150395
Biobank	rs373150395
1000 genomes	rs373150395
hgdp	rs373150395
ensembl	rs373150395
geneview	rs373150395
scholar	rs373150395
google	rs373150395
pharmgkb	rs373150395
gwascentral	rs373150395
openSNP	rs373150395
23andMe	rs373150395
SNPshot	rs373150395
SNPdbe	rs373150395
MSV3d	rs373150395
GWAS Ctlg	rs373150395

Max Magnitude

0

ClinVar
Risk	rs373150395(T;T)
Alt	rs373150395(T;T)
Reference	Rs373150395(C;C)
Significance	Pathogenic
Disease	not specified not provided
Variation	info
Gene	SCN4A
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000017.10:g.62025363C>T
CLNSRC
CLNACC	RCV000326941.1, RCV000438769.1,