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rs267607010

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607010(C;G)
Make rs267607010(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114497
GeneRET
is asnp
is mentioned by
dbSNPrs267607010
ebirs267607010
HLIrs267607010
Exacrs267607010
Varsomers267607010
Maprs267607010
PheGenIrs267607010
hapmaprs267607010
1000 genomesrs267607010
hgdprs267607010
ensemblrs267607010
gopubmedrs267607010
geneviewrs267607010
scholarrs267607010
googlers267607010
pharmgkbrs267607010
gwascentralrs267607010
openSNPrs267607010
23andMers267607010
23andMe allrs267607010
SNP Nexus

SNPshotrs267607010
SNPdbers267607010
MSV3drs267607010
GWAS Ctlgrs267607010
Max Magnitude0
ClinVar
Risk rs267607010(G;G)
Alt rs267607010(G;G)
Reference rs267607010(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a Multiple endocrine neoplasia, type 2
Reversed 0
HGVS NC_000010.10:g.43609945C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014920.25, RCV000196130.1,