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rs121912623

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912623(C;T)
Make rs121912623(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position74812322
GeneTRPM6
is asnp
is mentioned by
dbSNPrs121912623
ebirs121912623
HLIrs121912623
Exacrs121912623
Varsomers121912623
Maprs121912623
PheGenIrs121912623
hapmaprs121912623
1000 genomesrs121912623
hgdprs121912623
ensemblrs121912623
gopubmedrs121912623
geneviewrs121912623
scholarrs121912623
googlers121912623
pharmgkbrs121912623
gwascentralrs121912623
openSNPrs121912623
23andMers121912623
23andMe allrs121912623
SNP Nexus

SNPshotrs121912623
SNPdbers121912623
MSV3drs121912623
GWAS Ctlgrs121912623
Max Magnitude0
OMIM607009
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121912623(T;T)
Alt rs121912623(T;T)
Reference rs121912623(C;C)
Significance Pathogenic
Disease Hypomagnesemia 1
Variation info
Gene TRPM6
CLNDBN Hypomagnesemia 1, intestinal
Reversed 1
HGVS NC_000009.11:g.77427238G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003764.3,