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

rs377767409

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs377767409(GC;TG)
Make rs377767409(TG;TG)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114501
GeneRET
is asnp
is mentioned by
dbSNPrs377767409
ebirs377767409
HLIrs377767409
Exacrs377767409
Varsomers377767409
Maprs377767409
PheGenIrs377767409
hapmaprs377767409
1000 genomesrs377767409
hgdprs377767409
ensemblrs377767409
gopubmedrs377767409
geneviewrs377767409
scholarrs377767409
googlers377767409
pharmgkbrs377767409
gwascentralrs377767409
openSNPrs377767409
23andMers377767409
23andMe allrs377767409
SNP Nexus

SNPshotrs377767409
SNPdbers377767409
MSV3drs377767409
GWAS Ctlgrs377767409
Max Magnitude0
ClinVar
Risk rs377767409(TG;TG)
Alt rs377767409(TG;TG)
Reference rs377767409(GC;GC)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a
Reversed 0
HGVS NC_000010.10:g.43609949_43609950delGCinsTG
CLNSRC ClinVar
CLNACC RCV000021826.1,