Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223311

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223311(A;A)
Make rs863223311(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64805033
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs863223311
ebirs863223311
HLIrs863223311
Exacrs863223311
Varsomers863223311
Maprs863223311
PheGenIrs863223311
hapmaprs863223311
1000 genomesrs863223311
hgdprs863223311
ensemblrs863223311
gopubmedrs863223311
geneviewrs863223311
scholarrs863223311
googlers863223311
pharmgkbrs863223311
gwascentralrs863223311
openSNPrs863223311
23andMers863223311
23andMe allrs863223311
SNP Nexus

SNPshotrs863223311
SNPdbers863223311
MSV3drs863223311
GWAS Ctlgrs863223311
Max Magnitude0
ClinVar
Risk rs863223311(A;A)
Alt rs863223311(A;A)
Reference rs863223311(G;G)
Significance Pathogenic
Disease Hyperparathyroidism 1
Variation info
Gene MAP4K2 MEN1
CLNDBN Hyperparathyroidism 1
Reversed 1
HGVS NC_000011.9:g.64572505C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018187.2,