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rs794728688

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728688(A;A)
Make rs794728688(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position43123808
GeneRET
is asnp
is mentioned by
dbSNPrs794728688
ebirs794728688
HLIrs794728688
Exacrs794728688
Varsomers794728688
Maprs794728688
PheGenIrs794728688
hapmaprs794728688
1000 genomesrs794728688
hgdprs794728688
ensemblrs794728688
gopubmedrs794728688
geneviewrs794728688
scholarrs794728688
googlers794728688
pharmgkbrs794728688
gwascentralrs794728688
openSNPrs794728688
23andMers794728688
23andMe allrs794728688
SNP Nexus

SNPshotrs794728688
SNPdbers794728688
MSV3drs794728688
GWAS Ctlgrs794728688
Max Magnitude0
ClinVar
Risk rs794728688(A;A)
Alt rs794728688(A;A)
Reference rs794728688(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RET
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.43619256T>A
CLNSRC
CLNACC RCV000182589.1,