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rs377767398

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGC;TGC) 0 common in clinvar
Make rs377767398(AT;AT)
Make rs377767398(AT;GC)
Make rs377767398(GC;GC)
ReferenceGRCh38 38.1/141
Chromosome10
Position43113628
GeneRET
is asnp
is mentioned by
dbSNPrs377767398
ebirs377767398
HLIrs377767398
Exacrs377767398
Varsomers377767398
Maprs377767398
PheGenIrs377767398
hapmaprs377767398
1000 genomesrs377767398
hgdprs377767398
ensemblrs377767398
gopubmedrs377767398
geneviewrs377767398
scholarrs377767398
googlers377767398
pharmgkbrs377767398
gwascentralrs377767398
openSNPrs377767398
23andMers377767398
23andMe allrs377767398
SNP Nexus

SNPshotrs377767398
SNPdbers377767398
MSV3drs377767398
GWAS Ctlgrs377767398
Max Magnitude0
ClinVar
Risk rs377767398(TAT,TCT,TTT;TAT,TCT,TTT)
Alt rs377767398(TAT,TCT,TTT;TAT,TCT,TTT)
Reference rs377767398(TGC;TGC)
Significance Pathogenic
Disease MEN2 phenotype: Unclassified
Variation info
Gene RET
CLNDBN MEN2 phenotype: Unclassified
Reversed 0
HGVS NC_000010.10:g.43609076_43609077delGCinsAT; NC_000010.10:g.43609076_43609077delGCinsCT; NC_000010.10:g.43609076_43609077delGCinsTT
CLNSRC ClinVar
CLNACC RCV000021785.1, RCV000032028.1, RCV000032029.1,