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rs193922700

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922700(C;T)
Make rs193922700(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114680
GeneRET
is asnp
is mentioned by
dbSNPrs193922700
ebirs193922700
HLIrs193922700
Exacrs193922700
Varsomers193922700
Maprs193922700
PheGenIrs193922700
hapmaprs193922700
1000 genomesrs193922700
hgdprs193922700
ensemblrs193922700
gopubmedrs193922700
geneviewrs193922700
scholarrs193922700
googlers193922700
pharmgkbrs193922700
gwascentralrs193922700
openSNPrs193922700
23andMers193922700
23andMe allrs193922700
SNP Nexus

SNPshotrs193922700
SNPdbers193922700
MSV3drs193922700
GWAS Ctlgrs193922700
Max Magnitude0
ClinVar
Risk rs193922700(T;T)
Alt rs193922700(T;T)
Reference rs193922700(C;C)
Significance Probable-Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a
Reversed 0
HGVS NC_000010.10:g.43610128C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030406.1,