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rs104894265

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894265(A;A)
Make rs104894265(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position64805758
GeneMEN1
is asnp
is mentioned by
dbSNPrs104894265
ebirs104894265
HLIrs104894265
Exacrs104894265
Varsomers104894265
Maprs104894265
PheGenIrs104894265
hapmaprs104894265
1000 genomesrs104894265
hgdprs104894265
ensemblrs104894265
gopubmedrs104894265
geneviewrs104894265
scholarrs104894265
googlers104894265
pharmgkbrs104894265
gwascentralrs104894265
openSNPrs104894265
23andMers104894265
23andMe allrs104894265
SNP Nexus

SNPshotrs104894265
SNPdbers104894265
MSV3drs104894265
GWAS Ctlgrs104894265
Max Magnitude0
OMIM131100
Desc
Variant0029
Relatedalso
ClinVar
Risk rs104894265(A;A)
Alt rs104894265(A;A)
Reference rs104894265(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64573230G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018185.2,