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rs786205910

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205910(A;A)
Make rs786205910(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position102919549
GeneCNNM2
is asnp
is mentioned by
dbSNPrs786205910
ebirs786205910
HLIrs786205910
Exacrs786205910
Varsomers786205910
Maprs786205910
PheGenIrs786205910
hapmaprs786205910
1000 genomesrs786205910
hgdprs786205910
ensemblrs786205910
gopubmedrs786205910
geneviewrs786205910
scholarrs786205910
googlers786205910
pharmgkbrs786205910
gwascentralrs786205910
openSNPrs786205910
23andMers786205910
23andMe allrs786205910
SNP Nexus

SNPshotrs786205910
SNPdbers786205910
MSV3drs786205910
GWAS Ctlgrs786205910
Max Magnitude0
ClinVar
Risk rs786205910(A;A)
Alt rs786205910(A;A)
Reference rs786205910(G;G)
Significance Pathogenic
Disease Hypomagnesemia
Variation info
Gene CNNM2
CLNDBN Hypomagnesemia, seizures, and mental retardation
Reversed 0
HGVS NC_000010.10:g.104679306G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000172914.2,