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rs377767436

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs377767436(-;-)
Make rs377767436(-;ACGAGCTGTGCC)
Make rs377767436(ACGAGCTGTGCC;ACGAGCTGTGCC)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114503
GeneRET
is asnp
is mentioned by
dbSNPrs377767436
ebirs377767436
HLIrs377767436
Exacrs377767436
Varsomers377767436
Maprs377767436
PheGenIrs377767436
hapmaprs377767436
1000 genomesrs377767436
hgdprs377767436
ensemblrs377767436
gopubmedrs377767436
geneviewrs377767436
scholarrs377767436
googlers377767436
pharmgkbrs377767436
gwascentralrs377767436
openSNPrs377767436
23andMers377767436
23andMe allrs377767436
SNP Nexus

SNPshotrs377767436
SNPdbers377767436
MSV3drs377767436
GWAS Ctlgrs377767436
Max Magnitude0
ClinVar
Risk rs377767436(ACGAGCTGTGCC;ACGAGCTGTGCC)
Alt rs377767436(ACGAGCTGTGCC;ACGAGCTGTGCC)
Reference rs377767436(;)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a
Reversed 0
HGVS NC_000010.10:g.43609940_43609951dupACGAGCTGTGCC
CLNSRC ClinVar
CLNACC RCV000021829.1,