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rs794726858

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794726858(C;G)
Make rs794726858(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position102919286
GeneCNNM2
is asnp
is mentioned by
dbSNPrs794726858
ebirs794726858
HLIrs794726858
Exacrs794726858
Varsomers794726858
Maprs794726858
PheGenIrs794726858
hapmaprs794726858
1000 genomesrs794726858
hgdprs794726858
ensemblrs794726858
gopubmedrs794726858
geneviewrs794726858
scholarrs794726858
googlers794726858
pharmgkbrs794726858
gwascentralrs794726858
openSNPrs794726858
23andMers794726858
23andMe allrs794726858
SNP Nexus

SNPshotrs794726858
SNPdbers794726858
MSV3drs794726858
GWAS Ctlgrs794726858
Max Magnitude0
ClinVar
Risk rs794726858(G;G)
Alt rs794726858(G;G)
Reference rs794726858(C;C)
Significance Pathogenic
Disease Hypomagnesemia
Variation info
Gene CNNM2
CLNDBN Hypomagnesemia, seizures, and mental retardation
Reversed 0
HGVS NC_000010.10:g.104679043C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000172915.2,