rs267607011

Orientation

plus

Stabilized

plus

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

Make rs267607011(C;G)

Make rs267607011(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43120184

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs267607011
dbSNP (classic)	rs267607011
ClinGen	rs267607011
ebi	rs267607011
HLI	rs267607011
Exac	rs267607011
Gnomad	rs267607011
Varsome	rs267607011
LitVar	rs267607011
Map	rs267607011
PheGenI	rs267607011
Biobank	rs267607011
1000 genomes	rs267607011
hgdp	rs267607011
ensembl	rs267607011
geneview	rs267607011
scholar	rs267607011
google	rs267607011
pharmgkb	rs267607011
gwascentral	rs267607011
openSNP	rs267607011
23andMe	rs267607011
SNPshot	rs267607011
SNPdbe	rs267607011
MSV3d	rs267607011
GWAS Ctlg	rs267607011

Max Magnitude

0

ClinVar
Risk	rs267607011(G;G) rs267607011(T;T)
Alt	rs267607011(G;G) rs267607011(T;T)
Reference	Rs267607011(C;C)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia MEN2 phenotype: Unknown MEN2 phenotype: Unclassified
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2b MEN2 phenotype: Unknown MEN2 phenotype: Unclassified
Reversed	0
HGVS	NC_000010.10:g.43615632C>G; NC_000010.10:g.43615632C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014972.26, RCV000021877.1, RCV000021878.1,

[PMID 17895320] RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center.