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rs377767408

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCTGT;GCTGT) 0 common in clinvar
Make rs377767408(CGTGC;CGTGC)
Make rs377767408(CGTGC;GCTGT)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114496
GeneRET
is asnp
is mentioned by
dbSNPrs377767408
ebirs377767408
HLIrs377767408
Exacrs377767408
Varsomers377767408
Maprs377767408
PheGenIrs377767408
hapmaprs377767408
1000 genomesrs377767408
hgdprs377767408
ensemblrs377767408
gopubmedrs377767408
geneviewrs377767408
scholarrs377767408
googlers377767408
pharmgkbrs377767408
gwascentralrs377767408
openSNPrs377767408
23andMers377767408
23andMe allrs377767408
SNP Nexus

SNPshotrs377767408
SNPdbers377767408
MSV3drs377767408
GWAS Ctlgrs377767408
Max Magnitude0
ClinVar
Risk rs377767408(CGTGC;CGTGC)
Alt rs377767408(CGTGC;CGTGC)
Reference rs377767408(GCTGT;GCTGT)
Significance Pathogenic
Disease MEN2A and Unclassified
Variation info
Gene RET
CLNDBN MEN2A and Unclassified
Reversed 0
HGVS NC_000010.10:g.43609944_43609948delGCTGTinsCGTGC
CLNSRC ClinVar
CLNACC RCV000021819.1,