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rs77711105

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs77711105(A;A)
Make rs77711105(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43114542
GeneRET
is asnp
is mentioned by
dbSNPrs77711105
ebirs77711105
HLIrs77711105
Exacrs77711105
Varsomers77711105
Maprs77711105
PheGenIrs77711105
hapmaprs77711105
1000 genomesrs77711105
hgdprs77711105
ensemblrs77711105
gopubmedrs77711105
geneviewrs77711105
scholarrs77711105
googlers77711105
pharmgkbrs77711105
gwascentralrs77711105
openSNPrs77711105
23andMers77711105
23andMe allrs77711105
SNP Nexus

SNPshotrs77711105
SNPdbers77711105
MSV3drs77711105
GWAS Ctlgrs77711105
Max Magnitude0
OMIM164761
Desc
Variant0047
Relatedalso
ClinVar
Risk rs77711105(A;A)
Alt rs77711105(A;A)
Reference rs77711105(G;G)
Significance Other
Disease Multiple endocrine neoplasia MEN2 phenotype: Unknown not provided Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a MEN2 phenotype: Unknown not provided Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia, type 2
Reversed 0
HGVS NC_000010.10:g.43609990G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014976.28, RCV000021834.1, RCV000034767.1, RCV000163319.2, RCV000198828.3,