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rs387906531

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906531(C;C)
Make rs387906531(C;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114496
GeneRET
is asnp
is mentioned by
dbSNPrs387906531
ebirs387906531
HLIrs387906531
Exacrs387906531
Varsomers387906531
Maprs387906531
PheGenIrs387906531
hapmaprs387906531
1000 genomesrs387906531
hgdprs387906531
ensemblrs387906531
gopubmedrs387906531
geneviewrs387906531
scholarrs387906531
googlers387906531
pharmgkbrs387906531
gwascentralrs387906531
openSNPrs387906531
23andMers387906531
23andMe allrs387906531
SNP Nexus

SNPshotrs387906531
SNPdbers387906531
MSV3drs387906531
GWAS Ctlgrs387906531
Max Magnitude0
ClinVar
Risk rs387906531(C;C)
Alt rs387906531(C;C)
Reference rs387906531(G;G)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a
Reversed 0
HGVS NC_000010.10:g.43609944G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014920.25,