rs267607010

Orientation

plus

Stabilized

plus

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

Make rs267607010(C;G)

Make rs267607010(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114497

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs267607010
dbSNP (classic)	rs267607010
ClinGen	rs267607010
ebi	rs267607010
HLI	rs267607010
Exac	rs267607010
Gnomad	rs267607010
Varsome	rs267607010
LitVar	rs267607010
Map	rs267607010
PheGenI	rs267607010
Biobank	rs267607010
1000 genomes	rs267607010
hgdp	rs267607010
ensembl	rs267607010
geneview	rs267607010
scholar	rs267607010
google	rs267607010
pharmgkb	rs267607010
gwascentral	rs267607010
openSNP	rs267607010
23andMe	rs267607010
SNPshot	rs267607010
SNPdbe	rs267607010
MSV3d	rs267607010
GWAS Ctlg	rs267607010

Max Magnitude

0

ClinVar
Risk	rs267607010(G;G)
Alt	rs267607010(G;G)
Reference	Rs267607010(C;C)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia Multiple endocrine neoplasia Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2a Multiple endocrine neoplasia, type 2 Multiple endocrine neoplasia, type 2b
Reversed	0
HGVS	NC_000010.10:g.43609945C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014920.25, RCV000196130.1, RCV000410079.1, RCV000411153.1,