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rs104894262

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894262(A;A)
Make rs104894262(A;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64807994
GeneMEN1
is asnp
is mentioned by
dbSNPrs104894262
ebirs104894262
HLIrs104894262
Exacrs104894262
Varsomers104894262
Maprs104894262
PheGenIrs104894262
hapmaprs104894262
1000 genomesrs104894262
hgdprs104894262
ensemblrs104894262
gopubmedrs104894262
geneviewrs104894262
scholarrs104894262
googlers104894262
pharmgkbrs104894262
gwascentralrs104894262
openSNPrs104894262
23andMers104894262
23andMe allrs104894262
SNP Nexus

SNPshotrs104894262
SNPdbers104894262
MSV3drs104894262
GWAS Ctlgrs104894262
Max Magnitude0
OMIM131100
Desc
Variant0021
Relatedalso
ClinVar
Risk rs104894262(A;A)
Alt rs104894262(A;A)
Reference rs104894262(T;T)
Significance Pathogenic
Disease Hyperparathyroidism 1
Variation info
Gene MEN1
CLNDBN Hyperparathyroidism 1
Reversed 1
HGVS NC_000011.9:g.64575466A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018177.2,