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rs794728687

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728687(C;T)
Make rs794728687(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position43123706
GeneRET
is asnp
is mentioned by
dbSNPrs794728687
ebirs794728687
HLIrs794728687
Exacrs794728687
Varsomers794728687
Maprs794728687
PheGenIrs794728687
hapmaprs794728687
1000 genomesrs794728687
hgdprs794728687
ensemblrs794728687
gopubmedrs794728687
geneviewrs794728687
scholarrs794728687
googlers794728687
pharmgkbrs794728687
gwascentralrs794728687
openSNPrs794728687
23andMers794728687
23andMe allrs794728687
SNP Nexus

SNPshotrs794728687
SNPdbers794728687
MSV3drs794728687
GWAS Ctlgrs794728687
Max Magnitude0
ClinVar
Risk rs794728687(T;T)
Alt rs794728687(T;T)
Reference rs794728687(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RET
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.43619154C>T
CLNSRC
CLNACC RCV000182588.1,