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rs797045204

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045204(A;G)
Make rs797045204(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position74782398
GeneTRPM6
is asnp
is mentioned by
dbSNPrs797045204
ebirs797045204
HLIrs797045204
Exacrs797045204
Varsomers797045204
Maprs797045204
PheGenIrs797045204
hapmaprs797045204
1000 genomesrs797045204
hgdprs797045204
ensemblrs797045204
gopubmedrs797045204
geneviewrs797045204
scholarrs797045204
googlers797045204
pharmgkbrs797045204
gwascentralrs797045204
openSNPrs797045204
23andMers797045204
23andMe allrs797045204
SNP Nexus

SNPshotrs797045204
SNPdbers797045204
MSV3drs797045204
GWAS Ctlgrs797045204
Max Magnitude0
ClinVar
Risk rs797045204(G;G)
Alt rs797045204(G;G)
Reference rs797045204(A;A)
Significance Pathogenic
Disease Hypomagnesemia 1
Variation info
Gene TRPM6
CLNDBN Hypomagnesemia 1, intestinal
Reversed 1
HGVS NC_000009.11:g.77397314T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000193181.2,