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rs869312167

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312167(-;-)
Make rs869312167(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position64809958
GeneMEN1
is asnp
is mentioned by
dbSNPrs869312167
ebirs869312167
HLIrs869312167
Exacrs869312167
Varsomers869312167
Maprs869312167
PheGenIrs869312167
hapmaprs869312167
1000 genomesrs869312167
hgdprs869312167
ensemblrs869312167
gopubmedrs869312167
geneviewrs869312167
scholarrs869312167
googlers869312167
pharmgkbrs869312167
gwascentralrs869312167
openSNPrs869312167
23andMers869312167
23andMe allrs869312167
SNP Nexus

SNPshotrs869312167
SNPdbers869312167
MSV3drs869312167
GWAS Ctlgrs869312167
Max Magnitude0
ClinVar
Risk rs869312167(;)
Alt rs869312167(;)
Reference rs869312167(A;A)
Significance Pathogenic
Disease Primary hyperparathyroidism
Variation info
Gene MEN1
CLNDBN Primary hyperparathyroidism
Reversed 1
HGVS NC_000011.9:g.64577430delT
CLNSRC
CLNACC RCV000210355.1,