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rs377767426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377767426(C;G)
Make rs377767426(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43119694
GeneRET
is asnp
is mentioned by
dbSNPrs377767426
ebirs377767426
HLIrs377767426
Exacrs377767426
Varsomers377767426
Maprs377767426
PheGenIrs377767426
hapmaprs377767426
1000 genomesrs377767426
hgdprs377767426
ensemblrs377767426
gopubmedrs377767426
geneviewrs377767426
scholarrs377767426
googlers377767426
pharmgkbrs377767426
gwascentralrs377767426
openSNPrs377767426
23andMers377767426
23andMe allrs377767426
SNP Nexus

SNPshotrs377767426
SNPdbers377767426
MSV3drs377767426
GWAS Ctlgrs377767426
Max Magnitude0
ClinVar
Risk rs377767426(G;G)
Alt rs377767426(G;G)
Reference rs377767426(C;C)
Significance Pathogenic
Disease Unclassifed Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Unclassifed Multiple endocrine neoplasia, type 2
Reversed 0
HGVS NC_000010.10:g.43615142C>G
CLNSRC ClinVar
CLNACC RCV000021869.1, RCV000204335.2,