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rs377767405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377767405(A;A)
Make rs377767405(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114489
GeneRET
is asnp
is mentioned by
dbSNPrs377767405
ebirs377767405
HLIrs377767405
Exacrs377767405
Varsomers377767405
Maprs377767405
PheGenIrs377767405
hapmaprs377767405
1000 genomesrs377767405
hgdprs377767405
ensemblrs377767405
gopubmedrs377767405
geneviewrs377767405
scholarrs377767405
googlers377767405
pharmgkbrs377767405
gwascentralrs377767405
openSNPrs377767405
23andMers377767405
23andMe allrs377767405
SNP Nexus

SNPshotrs377767405
SNPdbers377767405
MSV3drs377767405
GWAS Ctlgrs377767405
Max Magnitude0
ClinVar
Risk rs377767405(A,C,T;A,C,T)
Alt rs377767405(A,C,T;A,C,T)
Reference rs377767405(G;G)
Significance Pathogenic
Disease MEN2A and Unclassified MEN2 phenotype: Unknown FMTC and Unclassified
Variation info
Gene RET
CLNDBN MEN2A and Unclassified MEN2 phenotype: Unknown FMTC and Unclassified
Reversed 0
HGVS NC_000010.10:g.43609937G>A; NC_000010.10:g.43609937G>C; NC_000010.10:g.43609937G>T
CLNSRC ClinVar
CLNACC RCV000021807.1, RCV000021808.1, RCV000021809.1,