rs80338955

Orientation

minus

Stabilized

minus

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

Make rs80338955(A;A)

Make rs80338955(A;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

63957473

Gene	LOC105371858, SCN4A

is a	snp
is	mentioned by
dbSNP	rs80338955
dbSNP (classic)	rs80338955
ClinGen	rs80338955
ebi	rs80338955
HLI	rs80338955
Exac	rs80338955
Gnomad	rs80338955
Varsome	rs80338955
LitVar	rs80338955
Map	rs80338955
PheGenI	rs80338955
Biobank	rs80338955
1000 genomes	rs80338955
hgdp	rs80338955
ensembl	rs80338955
geneview	rs80338955
scholar	rs80338955
google	rs80338955
pharmgkb	rs80338955
gwascentral	rs80338955
openSNP	rs80338955
23andMe	rs80338955
SNPshot	rs80338955
SNPdbe	rs80338955
MSV3d	rs80338955
GWAS Ctlg	rs80338955

Max Magnitude

0

ClinVar
Risk	rs80338955(A;A)
Alt	rs80338955(A;A)
Reference	Rs80338955(C;C)
Significance	Pathogenic
Disease	Hyperkalemic Periodic Paralysis Type 1
Variation	info
Gene	SCN4A
CLNDBN	Hyperkalemic Periodic Paralysis Type 1
Reversed	1
HGVS	NC_000017.10:g.62034833G>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020265.2,