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rs794728689

From SNPedia

Orientationplus
Make rs794728689(-;-)
Make rs794728689(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position43123715
GeneRET
is asnp
is mentioned by
dbSNPrs794728689
ebirs794728689
HLIrs794728689
Exacrs794728689
Varsomers794728689
Maprs794728689
PheGenIrs794728689
hapmaprs794728689
1000 genomesrs794728689
hgdprs794728689
ensemblrs794728689
gopubmedrs794728689
geneviewrs794728689
scholarrs794728689
googlers794728689
pharmgkbrs794728689
gwascentralrs794728689
openSNPrs794728689
23andMers794728689
23andMe allrs794728689
SNP Nexus

SNPshotrs794728689
SNPdbers794728689
MSV3drs794728689
GWAS Ctlgrs794728689
Max Magnitude
ClinVar
Risk rs794728689(;)
Alt rs794728689(;)
Reference rs794728689(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RET
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.43619163delG
CLNSRC
CLNACC RCV000182592.1,