rs972964381

Orientation

plus

Stabilized

plus

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

Make rs972964381(C;C)

Make rs972964381(C;T)

Make rs972964381(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

101143190

Gene

NALCN

is a	snp
is	mentioned by
dbSNP	rs972964381
dbSNP (classic)	rs972964381
ClinGen	rs972964381
ebi	rs972964381
HLI	rs972964381
Exac	rs972964381
Gnomad	rs972964381
Varsome	rs972964381
LitVar	rs972964381
Map	rs972964381
PheGenI	rs972964381
Biobank	rs972964381
1000 genomes	rs972964381
hgdp	rs972964381
ensembl	rs972964381
geneview	rs972964381
scholar	rs972964381
google	rs972964381
pharmgkb	rs972964381
gwascentral	rs972964381
openSNP	rs972964381
23andMe	rs972964381
SNPshot	rs972964381
SNPdbe	rs972964381
MSV3d	rs972964381
GWAS Ctlg	rs972964381

Max Magnitude

0

ClinVar
Risk	rs972964381(A;A)
Alt	rs972964381(A;A)
Reference	Rs972964381(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NALCN
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.101795541G>A
CLNSRC
CLNACC	RCV000423757.1,