rs104893720

Orientation

plus

Stabilized

plus

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

Make rs104893720(C;T)

Make rs104893720(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

190404779

Gene

CLDN16

is a	snp
is	mentioned by
dbSNP	rs104893720
dbSNP (classic)	rs104893720
ClinGen	rs104893720
ebi	rs104893720
HLI	rs104893720
Exac	rs104893720
Gnomad	rs104893720
Varsome	rs104893720
LitVar	rs104893720
Map	rs104893720
PheGenI	rs104893720
Biobank	rs104893720
1000 genomes	rs104893720
hgdp	rs104893720
ensembl	rs104893720
geneview	rs104893720
scholar	rs104893720
google	rs104893720
pharmgkb	rs104893720
gwascentral	rs104893720
openSNP	rs104893720
23andMe	rs104893720
SNPshot	rs104893720
SNPdbe	rs104893720
MSV3d	rs104893720
GWAS Ctlg	rs104893720

Max Magnitude

0

OMIM	603959
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893720(T;T)
Alt	rs104893720(T;T)
Reference	Rs104893720(C;C)
Significance	Pathogenic
Disease	Primary hypomagnesemia
Variation	info
Gene	CLDN16
CLNDBN	Primary hypomagnesemia
Reversed	0
HGVS	NC_000003.11:g.190122568C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006288.3,