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rs121912622

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912622(C;G)
Make rs121912622(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position74802138
GeneTRPM6
is asnp
is mentioned by
dbSNPrs121912622
ebirs121912622
HLIrs121912622
Exacrs121912622
Varsomers121912622
Maprs121912622
PheGenIrs121912622
hapmaprs121912622
1000 genomesrs121912622
hgdprs121912622
ensemblrs121912622
gopubmedrs121912622
geneviewrs121912622
scholarrs121912622
googlers121912622
pharmgkbrs121912622
gwascentralrs121912622
openSNPrs121912622
23andMers121912622
23andMe allrs121912622
SNP Nexus

SNPshotrs121912622
SNPdbers121912622
MSV3drs121912622
GWAS Ctlgrs121912622
Max Magnitude0
OMIM607009
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121912622(G;G)
Alt rs121912622(G;G)
Reference rs121912622(C;C)
Significance Pathogenic
Disease Hypomagnesemia 1
Variation info
Gene TRPM6
CLNDBN Hypomagnesemia 1, intestinal
Reversed 1
HGVS NC_000009.11:g.77417054G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003758.3,