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rs386134249

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134249(A;A)
Make rs386134249(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64805122
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs386134249
ebirs386134249
HLIrs386134249
Exacrs386134249
Varsomers386134249
Maprs386134249
PheGenIrs386134249
hapmaprs386134249
1000 genomesrs386134249
hgdprs386134249
ensemblrs386134249
gopubmedrs386134249
geneviewrs386134249
scholarrs386134249
googlers386134249
pharmgkbrs386134249
gwascentralrs386134249
openSNPrs386134249
23andMers386134249
23andMe allrs386134249
SNP Nexus

SNPshotrs386134249
SNPdbers386134249
MSV3drs386134249
GWAS Ctlgrs386134249
Max Magnitude0
ClinVar
Risk rs386134249(A;A)
Alt rs386134249(A;A)
Reference rs386134249(G;G)
Significance Pathogenic
Disease Multiple endocrine neoplasia not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN Multiple endocrine neoplasia, type 1 not provided
Reversed 1
HGVS NC_000011.9:g.64572594C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030196.1, RCV000182419.1,