rs757674263

Orientation

plus

Stabilized

plus

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

Make rs757674263(A;A)

Make rs757674263(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

101111216

Gene

NALCN

is a	snp
is	mentioned by
dbSNP	rs757674263
dbSNP (classic)	rs757674263
ClinGen	rs757674263
ebi	rs757674263
HLI	rs757674263
Exac	rs757674263
Gnomad	rs757674263
Varsome	rs757674263
LitVar	rs757674263
Map	rs757674263
PheGenI	rs757674263
Biobank	rs757674263
1000 genomes	rs757674263
hgdp	rs757674263
ensembl	rs757674263
geneview	rs757674263
scholar	rs757674263
google	rs757674263
pharmgkb	rs757674263
gwascentral	rs757674263
openSNP	rs757674263
23andMe	rs757674263
SNPshot	rs757674263
SNPdbe	rs757674263
MSV3d	rs757674263
GWAS Ctlg	rs757674263

Max Magnitude

0

ClinVar
Risk	rs757674263(A;A)
Alt	rs757674263(A;A)
Reference	Rs757674263(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	NALCN
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000013.10:g.101763567G>A
CLNSRC
CLNACC	RCV000210615.1,