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rs121912624

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912624(C;T)
Make rs121912624(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position74842330
GeneTRPM6
is asnp
is mentioned by
dbSNPrs121912624
ebirs121912624
HLIrs121912624
Exacrs121912624
Varsomers121912624
Maprs121912624
PheGenIrs121912624
hapmaprs121912624
1000 genomesrs121912624
hgdprs121912624
ensemblrs121912624
gopubmedrs121912624
geneviewrs121912624
scholarrs121912624
googlers121912624
pharmgkbrs121912624
gwascentralrs121912624
openSNPrs121912624
23andMers121912624
23andMe allrs121912624
SNP Nexus

SNPshotrs121912624
SNPdbers121912624
MSV3drs121912624
GWAS Ctlgrs121912624
Max Magnitude0
OMIM607009
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121912624(T;T)
Alt rs121912624(T;T)
Reference rs121912624(C;C)
Significance Pathogenic
Disease Hypomagnesemia 1
Variation info
Gene TRPM6
CLNDBN Hypomagnesemia 1, intestinal
Reversed 1
HGVS NC_000009.11:g.77457246G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003765.3,