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rs786205909

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205909(A;A)
Make rs786205909(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position102918844
GeneCNNM2
is asnp
is mentioned by
dbSNPrs786205909
ebirs786205909
HLIrs786205909
Exacrs786205909
Varsomers786205909
Maprs786205909
PheGenIrs786205909
hapmaprs786205909
1000 genomesrs786205909
hgdprs786205909
ensemblrs786205909
gopubmedrs786205909
geneviewrs786205909
scholarrs786205909
googlers786205909
pharmgkbrs786205909
gwascentralrs786205909
openSNPrs786205909
23andMers786205909
23andMe allrs786205909
SNP Nexus

SNPshotrs786205909
SNPdbers786205909
MSV3drs786205909
GWAS Ctlgrs786205909
Max Magnitude0
ClinVar
Risk rs786205909(A;A)
Alt rs786205909(A;A)
Reference rs786205909(G;G)
Significance Pathogenic
Disease Hypomagnesemia
Variation info
Gene CNNM2
CLNDBN Hypomagnesemia, seizures, and mental retardation
Reversed 0
HGVS NC_000010.10:g.104678601G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000172913.2,