Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728686

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728686(G;G)
Make rs794728686(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position43123700
GeneRET
is asnp
is mentioned by
dbSNPrs794728686
ebirs794728686
HLIrs794728686
Exacrs794728686
Varsomers794728686
Maprs794728686
PheGenIrs794728686
hapmaprs794728686
1000 genomesrs794728686
hgdprs794728686
ensemblrs794728686
gopubmedrs794728686
geneviewrs794728686
scholarrs794728686
googlers794728686
pharmgkbrs794728686
gwascentralrs794728686
openSNPrs794728686
23andMers794728686
23andMe allrs794728686
SNP Nexus

SNPshotrs794728686
SNPdbers794728686
MSV3drs794728686
GWAS Ctlgrs794728686
Max Magnitude0
ClinVar
Risk rs794728686(G;G)
Alt rs794728686(G;G)
Reference rs794728686(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RET
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.43619148T>G
CLNSRC
CLNACC RCV000182587.1,