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rs794728685

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728685(A;G)
Make rs794728685(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position43119680
GeneRET
is asnp
is mentioned by
dbSNPrs794728685
ebirs794728685
HLIrs794728685
Exacrs794728685
Varsomers794728685
Maprs794728685
PheGenIrs794728685
hapmaprs794728685
1000 genomesrs794728685
hgdprs794728685
ensemblrs794728685
gopubmedrs794728685
geneviewrs794728685
scholarrs794728685
googlers794728685
pharmgkbrs794728685
gwascentralrs794728685
openSNPrs794728685
23andMers794728685
23andMe allrs794728685
SNP Nexus

SNPshotrs794728685
SNPdbers794728685
MSV3drs794728685
GWAS Ctlgrs794728685
Max Magnitude0
ClinVar
Risk rs794728685(G;G)
Alt rs794728685(G;G)
Reference rs794728685(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RET
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.43615128A>G
CLNSRC
CLNACC RCV000182586.1,