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rs794728684

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728684(A;T)
Make rs794728684(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position43077259
GeneRET
is asnp
is mentioned by
dbSNPrs794728684
ebirs794728684
HLIrs794728684
Exacrs794728684
Varsomers794728684
Maprs794728684
PheGenIrs794728684
hapmaprs794728684
1000 genomesrs794728684
hgdprs794728684
ensemblrs794728684
gopubmedrs794728684
geneviewrs794728684
scholarrs794728684
googlers794728684
pharmgkbrs794728684
gwascentralrs794728684
openSNPrs794728684
23andMers794728684
23andMe allrs794728684
SNP Nexus

SNPshotrs794728684
SNPdbers794728684
MSV3drs794728684
GWAS Ctlgrs794728684
Max Magnitude0
ClinVar
Risk rs794728684(T;T)
Alt rs794728684(T;T)
Reference rs794728684(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RET
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.43572707A>T
CLNSRC
CLNACC RCV000182578.1,