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rs794728639

From SNPedia

Orientationminus
Make rs794728639(-;-)
Make rs794728639(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64809803
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728639
ebirs794728639
HLIrs794728639
Exacrs794728639
Varsomers794728639
Maprs794728639
PheGenIrs794728639
hapmaprs794728639
1000 genomesrs794728639
hgdprs794728639
ensemblrs794728639
gopubmedrs794728639
geneviewrs794728639
scholarrs794728639
googlers794728639
pharmgkbrs794728639
gwascentralrs794728639
openSNPrs794728639
23andMers794728639
23andMe allrs794728639
SNP Nexus

SNPshotrs794728639
SNPdbers794728639
MSV3drs794728639
GWAS Ctlgrs794728639
Max Magnitude
ClinVar
Risk rs794728639(;)
Alt rs794728639(;)
Reference rs794728639(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia not provided
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1 not provided
Reversed 1
HGVS NC_000011.9:g.64577275delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000018159.2, RCV000182435.1,