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rs377767428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377767428(A;A)
Make rs377767428(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43120120
GeneRET
is asnp
is mentioned by
dbSNPrs377767428
ebirs377767428
HLIrs377767428
Exacrs377767428
Varsomers377767428
Maprs377767428
PheGenIrs377767428
hapmaprs377767428
1000 genomesrs377767428
hgdprs377767428
ensemblrs377767428
gopubmedrs377767428
geneviewrs377767428
scholarrs377767428
googlers377767428
pharmgkbrs377767428
gwascentralrs377767428
openSNPrs377767428
23andMers377767428
23andMe allrs377767428
SNP Nexus

SNPshotrs377767428
SNPdbers377767428
MSV3drs377767428
GWAS Ctlgrs377767428
Max Magnitude0
ClinVar
Risk rs377767428(A;A)
Alt rs377767428(A;A)
Reference rs377767428(G;G)
Significance Pathogenic
Disease MEN2 phenotype: Unclassified
Variation info
Gene RET
CLNDBN MEN2 phenotype: Unclassified
Reversed 0
HGVS NC_000010.10:g.43615568G>A
CLNSRC ClinVar
CLNACC RCV000021872.1,