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rs794728691

From SNPedia

Orientationplus
Make rs794728691(-;-)
Make rs794728691(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position43123708
GeneRET
is asnp
is mentioned by
dbSNPrs794728691
ebirs794728691
HLIrs794728691
Exacrs794728691
Varsomers794728691
Maprs794728691
PheGenIrs794728691
hapmaprs794728691
1000 genomesrs794728691
hgdprs794728691
ensemblrs794728691
gopubmedrs794728691
geneviewrs794728691
scholarrs794728691
googlers794728691
pharmgkbrs794728691
gwascentralrs794728691
openSNPrs794728691
23andMers794728691
23andMe allrs794728691
SNP Nexus

SNPshotrs794728691
SNPdbers794728691
MSV3drs794728691
GWAS Ctlgrs794728691
Max Magnitude
ClinVar
Risk rs794728691(;)
Alt rs794728691(;)
Reference rs794728691(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RET
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.43619156delC
CLNSRC
CLNACC RCV000182597.1,