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rs77503355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs77503355(A;A)
Make rs77503355(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43113655
GeneRET
is asnp
is mentioned by
dbSNPrs77503355
ebirs77503355
HLIrs77503355
Exacrs77503355
Varsomers77503355
Maprs77503355
PheGenIrs77503355
hapmaprs77503355
1000 genomesrs77503355
hgdprs77503355
ensemblrs77503355
gopubmedrs77503355
geneviewrs77503355
scholarrs77503355
googlers77503355
pharmgkbrs77503355
gwascentralrs77503355
openSNPrs77503355
23andMers77503355
23andMe allrs77503355
SNP Nexus

SNPshotrs77503355
SNPdbers77503355
MSV3drs77503355
GWAS Ctlgrs77503355
Max Magnitude0
OMIM164761
Desc
Variant0024
Relatedalso
OMIM164761
Desc
Variant0041
Relatedalso
ClinVar
Risk rs77503355(A,C,T;A,C,T)
Alt rs77503355(A,C,T;A,C,T)
Reference rs77503355(G;G)
Significance Pathogenic
Disease Multiple endocrine neoplasia MEN2A and FMTC Familial medullary thyroid carcinoma Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2a MEN2A and FMTC Familial medullary thyroid carcinoma Multiple endocrine neoplasia, type 2
Reversed 0
HGVS NC_000010.10:g.43609103G>A; NC_000010.10:g.43609103G>C; NC_000010.10:g.43609103G>T
CLNSRC OMIM Allelic Variant HGMD
CLNACC RCV000014936.24, RCV000021801.1, RCV000014970.22, RCV000021802.1, RCV000014953.23, RCV000021803.1, RCV000153834.3, RCV000233944.1,