Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515385

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515385(-;-)
Make rs397515385(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position64809708
GeneMEN1
is asnp
is mentioned by
dbSNPrs397515385
ebirs397515385
HLIrs397515385
Exacrs397515385
Varsomers397515385
Maprs397515385
PheGenIrs397515385
hapmaprs397515385
1000 genomesrs397515385
hgdprs397515385
ensemblrs397515385
gopubmedrs397515385
geneviewrs397515385
scholarrs397515385
googlers397515385
pharmgkbrs397515385
gwascentralrs397515385
openSNPrs397515385
23andMers397515385
23andMe allrs397515385
SNP Nexus

SNPshotrs397515385
SNPdbers397515385
MSV3drs397515385
GWAS Ctlgrs397515385
Max Magnitude0
ClinVar
Risk rs397515385(;)
Alt rs397515385(;)
Reference rs397515385(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.64577180delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000018161.3, RCV000182436.1,