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rs376872829

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376872829(A;A)
Make rs376872829(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64808019
GeneMEN1
is asnp
is mentioned by
dbSNPrs376872829
ebirs376872829
HLIrs376872829
Exacrs376872829
Varsomers376872829
Maprs376872829
PheGenIrs376872829
hapmaprs376872829
1000 genomesrs376872829
hgdprs376872829
ensemblrs376872829
gopubmedrs376872829
geneviewrs376872829
scholarrs376872829
googlers376872829
pharmgkbrs376872829
gwascentralrs376872829
openSNPrs376872829
23andMers376872829
23andMe allrs376872829
SNP Nexus

SNPshotrs376872829
SNPdbers376872829
MSV3drs376872829
GWAS Ctlgrs376872829
Max Magnitude0
ClinVar
Risk rs376872829(A,G;A,G)
Alt rs376872829(A,G;A,G)
Reference rs376872829(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.64575491C>G
CLNSRC
CLNACC RCV000182408.1,