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rs864622615

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622615(C;T)
Make rs864622615(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64805171
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs864622615
ebirs864622615
HLIrs864622615
Exacrs864622615
Varsomers864622615
Maprs864622615
PheGenIrs864622615
hapmaprs864622615
1000 genomesrs864622615
hgdprs864622615
ensemblrs864622615
gopubmedrs864622615
geneviewrs864622615
scholarrs864622615
googlers864622615
pharmgkbrs864622615
gwascentralrs864622615
openSNPrs864622615
23andMers864622615
23andMe allrs864622615
SNP Nexus

SNPshotrs864622615
SNPdbers864622615
MSV3drs864622615
GWAS Ctlgrs864622615
Max Magnitude0
ClinVar
Risk rs864622615(T;T)
Alt rs864622615(T;T)
Reference rs864622615(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MAP4K2 MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64572643G>A
CLNSRC
CLNACC RCV000205609.1,