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rs794728642

From SNPedia

Orientationminus
Make rs794728642(-;-)
Make rs794728642(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804621
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728642
ebirs794728642
HLIrs794728642
Exacrs794728642
Varsomers794728642
Maprs794728642
PheGenIrs794728642
hapmaprs794728642
1000 genomesrs794728642
hgdprs794728642
ensemblrs794728642
gopubmedrs794728642
geneviewrs794728642
scholarrs794728642
googlers794728642
pharmgkbrs794728642
gwascentralrs794728642
openSNPrs794728642
23andMers794728642
23andMe allrs794728642
SNP Nexus

SNPshotrs794728642
SNPdbers794728642
MSV3drs794728642
GWAS Ctlgrs794728642
Max Magnitude
ClinVar
Risk rs794728642(;)
Alt rs794728642(;)
Reference rs794728642(C;C)
Significance Pathogenic
Disease not provided Multiple endocrine neoplasia
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64572093delG
CLNSRC
CLNACC RCV000182439.1, RCV000228926.1,