rs869312952

Orientation

minus

Stabilized

minus

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

Make rs869312952(A;A)

Make rs869312952(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

101073583

Gene

NALCN

is a	snp
is	mentioned by
dbSNP	rs869312952
dbSNP (classic)	rs869312952
ClinGen	rs869312952
ebi	rs869312952
HLI	rs869312952
Exac	rs869312952
Gnomad	rs869312952
Varsome	rs869312952
LitVar	rs869312952
Map	rs869312952
PheGenI	rs869312952
Biobank	rs869312952
1000 genomes	rs869312952
hgdp	rs869312952
ensembl	rs869312952
geneview	rs869312952
scholar	rs869312952
google	rs869312952
pharmgkb	rs869312952
gwascentral	rs869312952
openSNP	rs869312952
23andMe	rs869312952
SNPshot	rs869312952
SNPdbe	rs869312952
MSV3d	rs869312952
GWAS Ctlg	rs869312952

Max Magnitude

0

ClinVar
Risk	rs869312952(A;A)
Alt	rs869312952(A;A)
Reference	Rs869312952(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	NALCN
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000013.10:g.101725935C>T
CLNSRC
CLNACC	RCV000210682.1,