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rs377767429

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs377767429(GC;TT)
Make rs377767429(TT;TT)
ReferenceGRCh38 38.1/141
Chromosome10
Position43120120
GeneRET
is asnp
is mentioned by
dbSNPrs377767429
ebirs377767429
HLIrs377767429
Exacrs377767429
Varsomers377767429
Maprs377767429
PheGenIrs377767429
hapmaprs377767429
1000 genomesrs377767429
hgdprs377767429
ensemblrs377767429
gopubmedrs377767429
geneviewrs377767429
scholarrs377767429
googlers377767429
pharmgkbrs377767429
gwascentralrs377767429
openSNPrs377767429
23andMers377767429
23andMe allrs377767429
SNP Nexus

SNPshotrs377767429
SNPdbers377767429
MSV3drs377767429
GWAS Ctlgrs377767429
Max Magnitude0
ClinVar
Risk rs377767429(TT;TT)
Alt rs377767429(TT;TT)
Reference rs377767429(GC;GC)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2b
Reversed 0
HGVS NC_000010.10:g.43615568_43615569delGCinsTT
CLNSRC ClinVar
CLNACC RCV000021873.1,