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rs104894257

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs104894257(A;A)
Make rs104894257(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64807951
GeneMEN1
is asnp
is mentioned by
dbSNPrs104894257
ebirs104894257
HLIrs104894257
Exacrs104894257
Varsomers104894257
Maprs104894257
PheGenIrs104894257
hapmaprs104894257
1000 genomesrs104894257
hgdprs104894257
ensemblrs104894257
gopubmedrs104894257
geneviewrs104894257
scholarrs104894257
googlers104894257
pharmgkbrs104894257
gwascentralrs104894257
openSNPrs104894257
23andMers104894257
23andMe allrs104894257
SNP Nexus

SNPshotrs104894257
SNPdbers104894257
MSV3drs104894257
GWAS Ctlgrs104894257
Max Magnitude0
OMIM131100
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894257(A;A)
Alt rs104894257(A;A)
Reference rs104894257(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575423C>T
CLNSRC
CLNACC RCV000182450.1,