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rs377767437

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs377767437(-;-)
Make rs377767437(-;TGCCGCACG)
Make rs377767437(TGCCGCACG;TGCCGCACG)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114508
GeneRET
is asnp
is mentioned by
dbSNPrs377767437
ebirs377767437
HLIrs377767437
Exacrs377767437
Varsomers377767437
Maprs377767437
PheGenIrs377767437
hapmaprs377767437
1000 genomesrs377767437
hgdprs377767437
ensemblrs377767437
gopubmedrs377767437
geneviewrs377767437
scholarrs377767437
googlers377767437
pharmgkbrs377767437
gwascentralrs377767437
openSNPrs377767437
23andMers377767437
23andMe allrs377767437
SNP Nexus

SNPshotrs377767437
SNPdbers377767437
MSV3drs377767437
GWAS Ctlgrs377767437
Max Magnitude0
ClinVar
Risk rs377767437(GTGCCGCAC;GTGCCGCAC)
Alt rs377767437(GTGCCGCAC;GTGCCGCAC)
Reference rs377767437(;)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a
Reversed 0
HGVS NC_000010.10:g.43609948_43609956dupTGCCGCACG
CLNSRC ClinVar
CLNACC RCV000021831.1,