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rs104893732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893732(A;A)
Make rs104893732(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position190402362
GeneCLDN16
is asnp
is mentioned by
dbSNPrs104893732
ebirs104893732
HLIrs104893732
Exacrs104893732
Varsomers104893732
Maprs104893732
PheGenIrs104893732
hapmaprs104893732
1000 genomesrs104893732
hgdprs104893732
ensemblrs104893732
gopubmedrs104893732
geneviewrs104893732
scholarrs104893732
googlers104893732
pharmgkbrs104893732
gwascentralrs104893732
openSNPrs104893732
23andMers104893732
23andMe allrs104893732
SNP Nexus

SNPshotrs104893732
SNPdbers104893732
MSV3drs104893732
GWAS Ctlgrs104893732
Max Magnitude0
OMIM603959
Desc
Variant0013
Relatedalso
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 RCV000006300.2,