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rs77702891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs77702891(A;A)
Make rs77702891(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43106446
GeneLOC100288973, RET
is asnp
is mentioned by
dbSNPrs77702891
ebirs77702891
HLIrs77702891
Exacrs77702891
Varsomers77702891
Maprs77702891
PheGenIrs77702891
hapmaprs77702891
1000 genomesrs77702891
hgdprs77702891
ensemblrs77702891
gopubmedrs77702891
geneviewrs77702891
scholarrs77702891
googlers77702891
pharmgkbrs77702891
gwascentralrs77702891
openSNPrs77702891
23andMers77702891
23andMe allrs77702891
SNP Nexus

SNPshotrs77702891
SNPdbers77702891
MSV3drs77702891
GWAS Ctlgrs77702891
Max Magnitude0
OMIM164761
Desc
Variant0028
Relatedalso
ClinVar
Risk rs77702891(A;A)
Alt rs77702891(A;A)
Reference rs77702891(G;G)
Significance Other
Disease Hirschsprung disease 1
Variation info
Gene RET
CLNDBN Hirschsprung disease 1
Reversed 0
HGVS NC_000010.10:g.43601894G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014957.3,


[PMID 9111993] A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis.