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rs142318626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs142318626(C;T)
Make rs142318626(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position43119587
GeneRET
is asnp
is mentioned by
dbSNPrs142318626
dbSNP (old)rs142318626
ClinGenrs142318626
ebirs142318626
HLIrs142318626
Exacrs142318626
Gnomadrs142318626
Varsomers142318626
Maprs142318626
PheGenIrs142318626
Biobankrs142318626
1000 genomesrs142318626
hgdprs142318626
ensemblrs142318626
gopubmedrs142318626
geneviewrs142318626
scholarrs142318626
googlers142318626
pharmgkbrs142318626
gwascentralrs142318626
openSNPrs142318626
23andMers142318626
23andMe allrs142318626
SNPshotrs142318626
SNPdbers142318626
MSV3drs142318626
GWAS Ctlgrs142318626
Max Magnitude0
ClinVar
Risk rs142318626(T;T)
Alt rs142318626(T;T)
Reference Rs142318626(C;C)
Significance Probable-Pathogenic
Disease Multiple endocrine neoplasia Multiple endocrine neoplasia Multiple endocrine neoplasia not provided
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2 Multiple endocrine neoplasia, type 2a Multiple endocrine neoplasia, type 2b not provided
Reversed 0
HGVS NC_000010.10:g.43615035C>T
CLNSRC
CLNACC RCV000123311.3, RCV000409506.1, RCV000411874.1, RCV000414497.1,