rs9513851

Orientation

plus

Stabilized

plus

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

Make rs9513851(A;A)

Make rs9513851(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

101095633

Gene

NALCN

is a	snp
is	mentioned by
dbSNP	rs9513851
dbSNP (classic)	rs9513851
ClinGen	rs9513851
ebi	rs9513851
HLI	rs9513851
Exac	rs9513851
Gnomad	rs9513851
Varsome	rs9513851
LitVar	rs9513851
Map	rs9513851
PheGenI	rs9513851
Biobank	rs9513851
1000 genomes	rs9513851
hgdp	rs9513851
ensembl	rs9513851
geneview	rs9513851
scholar	rs9513851
google	rs9513851
pharmgkb	rs9513851
gwascentral	rs9513851
openSNP	rs9513851
23andMe	rs9513851
SNPshot	rs9513851
SNPdbe	rs9513851
MSV3d	rs9513851
GWAS Ctlg	rs9513851

GMAF

0.04545

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs9513851(A;A)
Alt	rs9513851(A;A)
Reference	Rs9513851(G;G)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	NALCN
CLNDBN	not specified
Reversed	0
HGVS	NC_000013.10:g.101747984G>A
CLNSRC
CLNACC	RCV000246356.1,