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

rs377767406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377767406(A;A)
Make rs377767406(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114491
GeneRET
is asnp
is mentioned by
dbSNPrs377767406
ebirs377767406
HLIrs377767406
Exacrs377767406
Varsomers377767406
Maprs377767406
PheGenIrs377767406
hapmaprs377767406
1000 genomesrs377767406
hgdprs377767406
ensemblrs377767406
gopubmedrs377767406
geneviewrs377767406
scholarrs377767406
googlers377767406
pharmgkbrs377767406
gwascentralrs377767406
openSNPrs377767406
23andMers377767406
23andMe allrs377767406
SNP Nexus

SNPshotrs377767406
SNPdbers377767406
MSV3drs377767406
GWAS Ctlgrs377767406
Max Magnitude0
ClinVar
Risk rs377767406(A,T;A,T)
Alt rs377767406(A,T;A,T)
Reference rs377767406(G;G)
Significance Pathogenic
Disease MEN2 phenotype: Unknown Multiple endocrine neoplasia Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene RET
CLNDBN MEN2 phenotype: Unknown Multiple endocrine neoplasia, type 2a Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000010.10:g.43609939G>A; NC_000010.10:g.43609939G>T
CLNSRC ClinVar
CLNACC RCV000021811.1, RCV000021812.1, RCV000219970.1,