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rs377767400

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377767400(C;G)
Make rs377767400(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43113650
GeneRET
is asnp
is mentioned by
dbSNPrs377767400
ebirs377767400
HLIrs377767400
Exacrs377767400
Varsomers377767400
Maprs377767400
PheGenIrs377767400
hapmaprs377767400
1000 genomesrs377767400
hgdprs377767400
ensemblrs377767400
gopubmedrs377767400
geneviewrs377767400
scholarrs377767400
googlers377767400
pharmgkbrs377767400
gwascentralrs377767400
openSNPrs377767400
23andMers377767400
23andMe allrs377767400
SNP Nexus

SNPshotrs377767400
SNPdbers377767400
MSV3drs377767400
GWAS Ctlgrs377767400
Max Magnitude0
ClinVar
Risk rs377767400(G;G)
Alt rs377767400(G;G)
Reference rs377767400(C;C)
Significance Pathogenic
Disease MEN2 phenotype: Unclassified
Variation info
Gene RET
CLNDBN MEN2 phenotype: Unclassified
Reversed 0
HGVS NC_000010.10:g.43609098C>G
CLNSRC ClinVar
CLNACC RCV000021796.1,