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rs386134260

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134260(C;G)
Make rs386134260(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position64806345
GeneMEN1
is asnp
is mentioned by
dbSNPrs386134260
ebirs386134260
HLIrs386134260
Exacrs386134260
Varsomers386134260
Maprs386134260
PheGenIrs386134260
hapmaprs386134260
1000 genomesrs386134260
hgdprs386134260
ensemblrs386134260
gopubmedrs386134260
geneviewrs386134260
scholarrs386134260
googlers386134260
pharmgkbrs386134260
gwascentralrs386134260
openSNPrs386134260
23andMers386134260
23andMe allrs386134260
SNP Nexus

SNPshotrs386134260
SNPdbers386134260
MSV3drs386134260
GWAS Ctlgrs386134260
Max Magnitude0
ClinVar
Risk rs386134260(G;G)
Alt rs386134260(G;G)
Reference rs386134260(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.64573817G>C
CLNSRC HGMD
CLNACC RCV000030210.2, RCV000082340.4,