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rs267607234

From SNPedia

Orientationminus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs267607234(AA;AA)
Make rs267607234(AA;GG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position64805745
GeneMEN1
is asnp
is mentioned by
dbSNPrs267607234
ebirs267607234
HLIrs267607234
Exacrs267607234
Varsomers267607234
Maprs267607234
PheGenIrs267607234
hapmaprs267607234
1000 genomesrs267607234
hgdprs267607234
ensemblrs267607234
gopubmedrs267607234
geneviewrs267607234
scholarrs267607234
googlers267607234
pharmgkbrs267607234
gwascentralrs267607234
openSNPrs267607234
23andMers267607234
23andMe allrs267607234
SNP Nexus

SNPshotrs267607234
SNPdbers267607234
MSV3drs267607234
GWAS Ctlgrs267607234
Max Magnitude0
ClinVar
Risk rs267607234(AA;AA)
Alt rs267607234(AA;AA)
Reference rs267607234(GG;GG)
Significance Pathogenic
Disease Angiofibroma
Variation info
Gene MEN1
CLNDBN Angiofibroma, somatic
Reversed 1
HGVS NC_000011.9:g.64573217_64573218delCCinsTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000018175.4,