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rs377767396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377767396(C;G)
Make rs377767396(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43113623
GeneRET
is asnp
is mentioned by
dbSNPrs377767396
ebirs377767396
HLIrs377767396
Exacrs377767396
Varsomers377767396
Maprs377767396
PheGenIrs377767396
hapmaprs377767396
1000 genomesrs377767396
hgdprs377767396
ensemblrs377767396
gopubmedrs377767396
geneviewrs377767396
scholarrs377767396
googlers377767396
pharmgkbrs377767396
gwascentralrs377767396
openSNPrs377767396
23andMers377767396
23andMe allrs377767396
SNP Nexus

SNPshotrs377767396
SNPdbers377767396
MSV3drs377767396
GWAS Ctlgrs377767396
Max Magnitude0
ClinVar
Risk rs377767396(G;G)
Alt rs377767396(G;G)
Reference rs377767396(C;C)
Significance Probable-Pathogenic
Disease No MEN2 disease
Variation info
Gene RET
CLNDBN No MEN2 disease
Reversed 0
HGVS NC_000010.10:g.43609071C>G
CLNSRC ClinVar
CLNACC RCV000021781.1,