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rs878855191

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855191(-;-)
Make rs878855191(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position64809787
GeneMEN1
is asnp
is mentioned by
dbSNPrs878855191
ebirs878855191
HLIrs878855191
Exacrs878855191
Varsomers878855191
Maprs878855191
PheGenIrs878855191
hapmaprs878855191
1000 genomesrs878855191
hgdprs878855191
ensemblrs878855191
gopubmedrs878855191
geneviewrs878855191
scholarrs878855191
googlers878855191
pharmgkbrs878855191
gwascentralrs878855191
openSNPrs878855191
23andMers878855191
23andMe allrs878855191
SNP Nexus

SNPshotrs878855191
SNPdbers878855191
MSV3drs878855191
GWAS Ctlgrs878855191
Max Magnitude0
ClinVar
Risk rs878855191(;)
Alt rs878855191(;)
Reference rs878855191(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.64577259delC
CLNSRC
CLNACC RCV000229514.1,