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rs878855192

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878855192(A;T)
Make rs878855192(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position64809752
GeneMEN1
is asnp
is mentioned by
dbSNPrs878855192
ebirs878855192
HLIrs878855192
Exacrs878855192
Varsomers878855192
Maprs878855192
PheGenIrs878855192
hapmaprs878855192
1000 genomesrs878855192
hgdprs878855192
ensemblrs878855192
gopubmedrs878855192
geneviewrs878855192
scholarrs878855192
googlers878855192
pharmgkbrs878855192
gwascentralrs878855192
openSNPrs878855192
23andMers878855192
23andMe allrs878855192
SNP Nexus

SNPshotrs878855192
SNPdbers878855192
MSV3drs878855192
GWAS Ctlgrs878855192
Max Magnitude0
ClinVar
Risk rs878855192(T;T)
Alt rs878855192(T;T)
Reference rs878855192(A;A)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64577224T>A
CLNSRC
CLNACC RCV000232425.1,