rs104893732

Orientation

plus

Stabilized

plus

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

Make rs104893732(A;A)

Make rs104893732(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

190402362

Gene

CLDN16

is a	snp
is	mentioned by
dbSNP	rs104893732
dbSNP (classic)	rs104893732
ClinGen	rs104893732
ebi	rs104893732
HLI	rs104893732
Exac	rs104893732
Gnomad	rs104893732
Varsome	rs104893732
LitVar	rs104893732
Map	rs104893732
PheGenI	rs104893732
Biobank	rs104893732
1000 genomes	rs104893732
hgdp	rs104893732
ensembl	rs104893732
geneview	rs104893732
scholar	rs104893732
google	rs104893732
pharmgkb	rs104893732
gwascentral	rs104893732
openSNP	rs104893732
23andMe	rs104893732
SNPshot	rs104893732
SNPdbe	rs104893732
MSV3d	rs104893732
GWAS Ctlg	rs104893732

Max Magnitude

0

OMIM	603959
Desc
Variant	0013
Related	also

ClinVar
Risk	rs104893732(A;A)
Alt	rs104893732(A;A)
Reference	Rs104893732(G;G)
Significance	Pathogenic
Disease	Primary hypomagnesemia
Variation	info
Gene	CLDN16
CLNDBN	Primary hypomagnesemia
Reversed	0
HGVS	NC_000003.11:g.190120151G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006300.3,