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rs104894256

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894256(G;G)
Make rs104894256(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64810045
GeneMEN1
is asnp
is mentioned by
dbSNPrs104894256
ebirs104894256
HLIrs104894256
Exacrs104894256
Varsomers104894256
Maprs104894256
PheGenIrs104894256
hapmaprs104894256
1000 genomesrs104894256
hgdprs104894256
ensemblrs104894256
gopubmedrs104894256
geneviewrs104894256
scholarrs104894256
googlers104894256
pharmgkbrs104894256
gwascentralrs104894256
openSNPrs104894256
23andMers104894256
23andMe allrs104894256
SNP Nexus

SNPshotrs104894256
SNPdbers104894256
MSV3drs104894256
GWAS Ctlgrs104894256
Max Magnitude0
OMIM131100
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894256(G;G)
Alt rs104894256(G;G)
Reference rs104894256(T;T)
Significance Pathogenic
Disease Multiple endocrine neoplasia not provided
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1 not provided
Reversed 1
HGVS NC_000011.9:g.64577517A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000018157.2, RCV000182402.1,