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rs863224526

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224526(G;T)
Make rs863224526(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804738
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs863224526
ebirs863224526
HLIrs863224526
Exacrs863224526
Varsomers863224526
Maprs863224526
PheGenIrs863224526
hapmaprs863224526
1000 genomesrs863224526
hgdprs863224526
ensemblrs863224526
gopubmedrs863224526
geneviewrs863224526
scholarrs863224526
googlers863224526
pharmgkbrs863224526
gwascentralrs863224526
openSNPrs863224526
23andMers863224526
23andMe allrs863224526
SNP Nexus

SNPshotrs863224526
SNPdbers863224526
MSV3drs863224526
GWAS Ctlgrs863224526
Max Magnitude0
ClinVar
Risk rs863224526(T;T)
Alt rs863224526(T;T)
Reference rs863224526(G;G)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MAP4K2 MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64572210C>A
CLNSRC
CLNACC RCV000198067.2,