rs878853133

Orientation

minus

Stabilized

minus

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

Make rs878853133(A;A)

Make rs878853133(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

101292058

Gene

NALCN

is a	snp
is	mentioned by
dbSNP	rs878853133
dbSNP (classic)	rs878853133
ClinGen	rs878853133
ebi	rs878853133
HLI	rs878853133
Exac	rs878853133
Gnomad	rs878853133
Varsome	rs878853133
LitVar	rs878853133
Map	rs878853133
PheGenI	rs878853133
Biobank	rs878853133
1000 genomes	rs878853133
hgdp	rs878853133
ensembl	rs878853133
geneview	rs878853133
scholar	rs878853133
google	rs878853133
pharmgkb	rs878853133
gwascentral	rs878853133
openSNP	rs878853133
23andMe	rs878853133
SNPshot	rs878853133
SNPdbe	rs878853133
MSV3d	rs878853133
GWAS Ctlg	rs878853133

Max Magnitude

0

ClinVar
Risk	rs878853133(A;A)
Alt	rs878853133(A;A)
Reference	Rs878853133(G;G)
Significance	Pathogenic
Disease	Congenital contractures of the limbs and face
Variation	info
Gene	NALCN
CLNDBN	Congenital contractures of the limbs and face, hypotonia, and developmental delay
Reversed	1
HGVS	NC_000013.10:g.101944409C>T
CLNSRC
CLNACC	RCV000224921.1,