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rs377767416

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs377767416(A;G)
Make rs377767416(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43118430
GeneRET
is asnp
is mentioned by
dbSNPrs377767416
ebirs377767416
HLIrs377767416
Exacrs377767416
Varsomers377767416
Maprs377767416
PheGenIrs377767416
hapmaprs377767416
1000 genomesrs377767416
hgdprs377767416
ensemblrs377767416
gopubmedrs377767416
geneviewrs377767416
scholarrs377767416
googlers377767416
pharmgkbrs377767416
gwascentralrs377767416
openSNPrs377767416
23andMers377767416
23andMe allrs377767416
SNP Nexus

SNPshotrs377767416
SNPdbers377767416
MSV3drs377767416
GWAS Ctlgrs377767416
Max Magnitude0
ClinVar
Risk rs377767416(G;G)
Alt rs377767416(G;G)
Reference rs377767416(A;A)
Significance Pathogenic
Disease MEN2 phenotype: Unclassified Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN MEN2 phenotype: Unclassified Multiple endocrine neoplasia, type 2
Reversed 0
HGVS NC_000010.10:g.43613878A>G
CLNSRC ClinVar
CLNACC RCV000021848.1, RCV000232536.1,