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rs1060499646

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499646(A;G)
Make rs1060499646(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position74792667
GeneTRPM6
is asnp
is mentioned by
dbSNPrs1060499646
dbSNP (old)rs1060499646
ClinGenrs1060499646
ebirs1060499646
HLIrs1060499646
Exacrs1060499646
Gnomadrs1060499646
Varsomers1060499646
LitVarrs1060499646
Maprs1060499646
PheGenIrs1060499646
Biobankrs1060499646
1000 genomesrs1060499646
hgdprs1060499646
ensemblrs1060499646
gopubmedrs1060499646
geneviewrs1060499646
scholarrs1060499646
googlers1060499646
pharmgkbrs1060499646
gwascentralrs1060499646
openSNPrs1060499646
23andMers1060499646
23andMe allrs1060499646
SNPshotrs1060499646
SNPdbers1060499646
MSV3drs1060499646
GWAS Ctlgrs1060499646
Max Magnitude0
ClinVar
Risk rs1060499646(G;G)
Alt rs1060499646(G;G)
Reference Rs1060499646(A;A)
Significance Probable-Pathogenic
Disease Hypomagnesemia 1
Variation info
Gene TRPM6
CLNDBN Hypomagnesemia 1, intestinal
Reversed 1
HGVS NC_000009.11:g.77407583T>C
CLNSRC
CLNACC RCV000463560.1,