rs76262710

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs76262710(C;C)

Make rs76262710(C;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43113648

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs76262710
dbSNP (classic)	rs76262710
ClinGen	rs76262710
ebi	rs76262710
HLI	rs76262710
Exac	rs76262710
Gnomad	rs76262710
Varsome	rs76262710
LitVar	rs76262710
Map	rs76262710
PheGenI	rs76262710
Biobank	rs76262710
1000 genomes	rs76262710
hgdp	rs76262710
ensembl	rs76262710
geneview	rs76262710
scholar	rs76262710
google	rs76262710
pharmgkb	rs76262710
gwascentral	rs76262710
openSNP	rs76262710
23andMe	rs76262710
SNPshot	rs76262710
SNPdbe	rs76262710
MSV3d	rs76262710
GWAS Ctlg	rs76262710

Max Magnitude

0

OMIM	164761
Desc
Variant	0001
Related	also

OMIM	164761
Desc
Variant	0025
Related	also

ClinVar
Risk	rs76262710(A;A) rs76262710(C;C) rs76262710(G;G)
Alt	rs76262710(A;A) rs76262710(C;C) rs76262710(G;G)
Reference	Rs76262710(T;T)
Significance	Other
Disease	MEN2A and FMTC not provided Familial medullary thyroid carcinoma Multiple endocrine neoplasia Multiple endocrine neoplasia Multiple endocrine neoplasia Medullary thyroid carcinoma Multiple endocrine neoplasia MEN2A and Unclassified Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	MEN2A and FMTC not provided Familial medullary thyroid carcinoma Multiple endocrine neoplasia, type 2a Multiple endocrine neoplasia, type 2b Multiple endocrine neoplasia, type 1 Medullary thyroid carcinoma Multiple endocrine neoplasia, type 4 MEN2A and Unclassified Multiple endocrine neoplasia, type 2
Reversed	0
HGVS	NC_000010.10:g.43609096T>A; NC_000010.10:g.43609096T>C; NC_000010.10:g.43609096T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000032040.1, RCV000182594.2, RCV000014954.26, RCV000021792.1, RCV000114391.3, RCV000345209.1, RCV000427260.1, RCV000434685.1, RCV000442341.1, RCV000444839.1, RCV000014919.21, RCV000021793.1, RCV000228834.2,

[PMID 3078962] Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains.

[PMID 7907913] Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC. [PMID 8103403] Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.