rs1064794722

Orientation

minus

Stabilized

minus

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

Chromosome

13

Position

101192008

Gene

NALCN

is a	snp
is	mentioned by
dbSNP	rs1064794722
dbSNP (classic)	rs1064794722
ClinGen	rs1064794722
ebi	rs1064794722
HLI	rs1064794722
Exac	rs1064794722
Gnomad	rs1064794722
Varsome	rs1064794722
LitVar	rs1064794722
Map	rs1064794722
PheGenI	rs1064794722
Biobank	rs1064794722
1000 genomes	rs1064794722
hgdp	rs1064794722
ensembl	rs1064794722
geneview	rs1064794722
scholar	rs1064794722
google	rs1064794722
pharmgkb	rs1064794722
gwascentral	rs1064794722
openSNP	rs1064794722
23andMe	rs1064794722
SNPshot	rs1064794722
SNPdbe	rs1064794722
MSV3d	rs1064794722
GWAS Ctlg	rs1064794722

Max Magnitude

0

ClinVar
Risk	rs1064794722(G;G)
Alt	rs1064794722(G;G)
Reference	Rs1064794722(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NALCN
CLNDBN	not provided
Reversed	1
HGVS	NC_000013.10:g.101844359T>C
CLNSRC
CLNACC	RCV000483143.1,