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rs121912625

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912625(C;T)
Make rs121912625(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position74840146
GeneTRPM6
is asnp
is mentioned by
dbSNPrs121912625
ebirs121912625
HLIrs121912625
Exacrs121912625
Varsomers121912625
Maprs121912625
PheGenIrs121912625
hapmaprs121912625
1000 genomesrs121912625
hgdprs121912625
ensemblrs121912625
gopubmedrs121912625
geneviewrs121912625
scholarrs121912625
googlers121912625
pharmgkbrs121912625
gwascentralrs121912625
openSNPrs121912625
23andMers121912625
23andMe allrs121912625
SNP Nexus

SNPshotrs121912625
SNPdbers121912625
MSV3drs121912625
GWAS Ctlgrs121912625
Max Magnitude0
OMIM607009
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121912625(T;T)
Alt rs121912625(T;T)
Reference rs121912625(C;C)
Significance Pathogenic
Disease Hypomagnesemia 1
Variation info
Gene TRPM6
CLNDBN Hypomagnesemia 1, intestinal
Reversed 1
HGVS NC_000009.11:g.77455062G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003768.3,