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rs863224527

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224527(A;A)
Make rs863224527(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804503
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs863224527
ebirs863224527
HLIrs863224527
Exacrs863224527
Varsomers863224527
Maprs863224527
PheGenIrs863224527
hapmaprs863224527
1000 genomesrs863224527
hgdprs863224527
ensemblrs863224527
gopubmedrs863224527
geneviewrs863224527
scholarrs863224527
googlers863224527
pharmgkbrs863224527
gwascentralrs863224527
openSNPrs863224527
23andMers863224527
23andMe allrs863224527
SNP Nexus

SNPshotrs863224527
SNPdbers863224527
MSV3drs863224527
GWAS Ctlgrs863224527
Max Magnitude0
ClinVar
Risk rs863224527(A;A)
Alt rs863224527(A;A)
Reference rs863224527(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.64571975C>T
CLNSRC
CLNACC RCV000199920.1,