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rs104894258

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs104894258(A;A)
Make rs104894258(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64807952
GeneMEN1
is asnp
is mentioned by
dbSNPrs104894258
ebirs104894258
HLIrs104894258
Exacrs104894258
Varsomers104894258
Maprs104894258
PheGenIrs104894258
hapmaprs104894258
1000 genomesrs104894258
hgdprs104894258
ensemblrs104894258
gopubmedrs104894258
geneviewrs104894258
scholarrs104894258
googlers104894258
pharmgkbrs104894258
gwascentralrs104894258
openSNPrs104894258
23andMers104894258
23andMe allrs104894258
SNP Nexus

SNPshotrs104894258
SNPdbers104894258
MSV3drs104894258
GWAS Ctlgrs104894258
Max Magnitude0
OMIM131100
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894258(A;A)
Alt rs104894258(A;A)
Reference rs104894258(G;G)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64575424C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018162.2,