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rs377767404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs377767404(C;C)
Make rs377767404(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114488
GeneRET
is asnp
is mentioned by
dbSNPrs377767404
ebirs377767404
HLIrs377767404
Exacrs377767404
Varsomers377767404
Maprs377767404
PheGenIrs377767404
hapmaprs377767404
1000 genomesrs377767404
hgdprs377767404
ensemblrs377767404
gopubmedrs377767404
geneviewrs377767404
scholarrs377767404
googlers377767404
pharmgkbrs377767404
gwascentralrs377767404
openSNPrs377767404
23andMers377767404
23andMe allrs377767404
SNP Nexus

SNPshotrs377767404
SNPdbers377767404
MSV3drs377767404
GWAS Ctlgrs377767404
Max Magnitude0
ClinVar
Risk rs377767404(C;C)
Alt rs377767404(C;C)
Reference rs377767404(T;T)
Significance Pathogenic
Disease MEN2A and FMTC
Variation info
Gene RET
CLNDBN MEN2A and FMTC
Reversed 0
HGVS NC_000010.10:g.43609936T>C
CLNSRC ClinVar
CLNACC RCV000021806.1,