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rs869025214

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025214(A;A)
Make rs869025214(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position74788613
GeneTRPM6
is asnp
is mentioned by
dbSNPrs869025214
ebirs869025214
HLIrs869025214
Exacrs869025214
Varsomers869025214
Maprs869025214
PheGenIrs869025214
hapmaprs869025214
1000 genomesrs869025214
hgdprs869025214
ensemblrs869025214
gopubmedrs869025214
geneviewrs869025214
scholarrs869025214
googlers869025214
pharmgkbrs869025214
gwascentralrs869025214
openSNPrs869025214
23andMers869025214
23andMe allrs869025214
SNP Nexus

SNPshotrs869025214
SNPdbers869025214
MSV3drs869025214
GWAS Ctlgrs869025214
Max Magnitude0
ClinVar
Risk rs869025214(A;A)
Alt rs869025214(A;A)
Reference rs869025214(G;G)
Significance Pathogenic
Disease Hypomagnesemia 1
Variation info
Gene TRPM6
CLNDBN Hypomagnesemia 1, intestinal
Reversed 1
HGVS NC_000009.11:g.77403529C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000207483.2,