Have questions? Visit https://www.reddit.com/r/SNPedia

rs532862288

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs532862288(C;T)
Make rs532862288(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position43128238
GeneRET
is asnp
is mentioned by
dbSNPrs532862288
ebirs532862288
HLIrs532862288
Exacrs532862288
Varsomers532862288
Maprs532862288
PheGenIrs532862288
hapmaprs532862288
1000 genomesrs532862288
hgdprs532862288
ensemblrs532862288
gopubmedrs532862288
geneviewrs532862288
scholarrs532862288
googlers532862288
pharmgkbrs532862288
gwascentralrs532862288
openSNPrs532862288
23andMers532862288
23andMe allrs532862288
SNP Nexus

SNPshotrs532862288
SNPdbers532862288
MSV3drs532862288
GWAS Ctlgrs532862288
Max Magnitude0
ClinVar
Risk rs532862288(T;T)
Alt rs532862288(T;T)
Reference rs532862288(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RET
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.43623686C>T
CLNSRC
CLNACC RCV000182591.1,