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rs869025185

From SNPedia

Orientationminus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs869025185(-;-)
Make rs869025185(-;GAG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position64805731
GeneMEN1
is asnp
is mentioned by
dbSNPrs869025185
ebirs869025185
HLIrs869025185
Exacrs869025185
Varsomers869025185
Maprs869025185
PheGenIrs869025185
hapmaprs869025185
1000 genomesrs869025185
hgdprs869025185
ensemblrs869025185
gopubmedrs869025185
geneviewrs869025185
scholarrs869025185
googlers869025185
pharmgkbrs869025185
gwascentralrs869025185
openSNPrs869025185
23andMers869025185
23andMe allrs869025185
SNP Nexus

SNPshotrs869025185
SNPdbers869025185
MSV3drs869025185
GWAS Ctlgrs869025185
Max Magnitude0
ClinVar
Risk rs869025185(;)
Alt rs869025185(;)
Reference rs869025185(GAG;GAG)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64573203_64573205delCTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000018165.2,