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rs377767389

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs377767389(CT;CT)
Make rs377767389(CT;GC)
ReferenceGRCh38 38.1/141
Chromosome10
Position43112120
GeneRET
is asnp
is mentioned by
dbSNPrs377767389
ebirs377767389
HLIrs377767389
Exacrs377767389
Varsomers377767389
Maprs377767389
PheGenIrs377767389
hapmaprs377767389
1000 genomesrs377767389
hgdprs377767389
ensemblrs377767389
gopubmedrs377767389
geneviewrs377767389
scholarrs377767389
googlers377767389
pharmgkbrs377767389
gwascentralrs377767389
openSNPrs377767389
23andMers377767389
23andMe allrs377767389
SNP Nexus

SNPshotrs377767389
SNPdbers377767389
MSV3drs377767389
GWAS Ctlgrs377767389
Max Magnitude0
ClinVar
Risk rs377767389(CT;CT)
Alt rs377767389(CT;CT)
Reference rs377767389(GC;GC)
Significance Pathogenic
Disease MEN2 phenotype: Unclassified
Variation info
Gene RET
CLNDBN MEN2 phenotype: Unclassified
Reversed 0
HGVS NC_000010.10:g.43607568_43607569delGCinsCT
CLNSRC ClinVar
CLNACC RCV000021765.1,