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rs794727130

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATGCAGT;ATGCAGT) 0 common in clinvar
Make rs794727130(-;-)
Make rs794727130(-;GCAGTAT)
Make rs794727130(GCAGTAT;GCAGTAT)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position43119724
GeneRET
is asnp
is mentioned by
dbSNPrs794727130
ClinGenrs794727130
ebirs794727130
HLIrs794727130
Exacrs794727130
Varsomers794727130
Maprs794727130
PheGenIrs794727130
hapmaprs794727130
1000 genomesrs794727130
hgdprs794727130
ensemblrs794727130
gopubmedrs794727130
geneviewrs794727130
scholarrs794727130
googlers794727130
pharmgkbrs794727130
gwascentralrs794727130
openSNPrs794727130
23andMers794727130
23andMe allrs794727130
SNP Nexus

SNPshotrs794727130
SNPdbers794727130
MSV3drs794727130
GWAS Ctlgrs794727130
Max Magnitude0
ClinVar
Risk rs794727130(-;-)
Alt rs794727130(-;-)
Reference Rs794727130(ATGCAGT;ATGCAGT)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a
Reversed 0
HGVS NC_000010.10:g.43615172_43615178delGCAGTAT
CLNSRC
CLNACC RCV000174791.1,