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rs377767438

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs377767438(A;GACCTGTGCCGCC)
Make rs377767438(GACCTGTGCCGCC;GACCTGTGCCGCC)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114506
GeneRET
is asnp
is mentioned by
dbSNPrs377767438
ebirs377767438
HLIrs377767438
Exacrs377767438
Varsomers377767438
Maprs377767438
PheGenIrs377767438
hapmaprs377767438
1000 genomesrs377767438
hgdprs377767438
ensemblrs377767438
gopubmedrs377767438
geneviewrs377767438
scholarrs377767438
googlers377767438
pharmgkbrs377767438
gwascentralrs377767438
openSNPrs377767438
23andMers377767438
23andMe allrs377767438
SNP Nexus

SNPshotrs377767438
SNPdbers377767438
MSV3drs377767438
GWAS Ctlgrs377767438
Max Magnitude0
ClinVar
Risk rs377767438(GACCTGTGCCGCC;GACCTGTGCCGCC)
Alt rs377767438(GACCTGTGCCGCC;GACCTGTGCCGCC)
Reference rs377767438(A;A)
Significance Pathogenic
Disease MEN2 phenotype: Unclassified
Variation info
Gene RET
CLNDBN MEN2 phenotype: Unclassified
Reversed 0
HGVS NC_000010.10:g.43609954delAinsGACCTGTGCCGCC
CLNSRC ClinVar
CLNACC RCV000021830.1,