Have questions? Visit https://www.reddit.com/r/SNPedia

rs377767440

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377767440(G;TTCT)
Make rs377767440(TTCT;TTCT)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114598
GeneRET
is asnp
is mentioned by
dbSNPrs377767440
ebirs377767440
HLIrs377767440
Exacrs377767440
Varsomers377767440
Maprs377767440
PheGenIrs377767440
hapmaprs377767440
1000 genomesrs377767440
hgdprs377767440
ensemblrs377767440
gopubmedrs377767440
geneviewrs377767440
scholarrs377767440
googlers377767440
pharmgkbrs377767440
gwascentralrs377767440
openSNPrs377767440
23andMers377767440
23andMe allrs377767440
SNP Nexus

SNPshotrs377767440
SNPdbers377767440
MSV3drs377767440
GWAS Ctlgrs377767440
Max Magnitude0
ClinVar
Risk rs377767440(TTCT;TTCT)
Alt rs377767440(TTCT;TTCT)
Reference rs377767440(G;G)
Significance Pathogenic
Disease MEN2A and Unclassified
Variation info
Gene RET
CLNDBN MEN2A and Unclassified
Reversed 0
HGVS NC_000010.10:g.43610046delGinsTTCT
CLNSRC ClinVar
CLNACC RCV000021840.1,