rs377767400

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	5.1	Multiple Endocrine Neoplasia IIA

Make rs377767400(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43113650

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767400
dbSNP (classic)	rs377767400
ClinGen	rs377767400
ebi	rs377767400
HLI	rs377767400
Exac	rs377767400
Gnomad	rs377767400
Varsome	rs377767400
LitVar	rs377767400
Map	rs377767400
PheGenI	rs377767400
Biobank	rs377767400
1000 genomes	rs377767400
hgdp	rs377767400
ensembl	rs377767400
geneview	rs377767400
scholar	rs377767400
google	rs377767400
pharmgkb	rs377767400
gwascentral	rs377767400
openSNP	rs377767400
23andMe	rs377767400
SNPshot	rs377767400
SNPdbe	rs377767400
MSV3d	rs377767400
GWAS Ctlg	rs377767400

Max Magnitude

5.1

ClinVar
Risk	rs377767400(G;G)
Alt	rs377767400(G;G)
Reference	Rs377767400(C;C)
Significance	Pathogenic
Disease	MEN2 phenotype: Unclassified
Variation	info
Gene	RET
CLNDBN	MEN2 phenotype: Unclassified
Reversed	0
HGVS	NC_000010.10:g.43609098C>G
CLNSRC	ClinVar
CLNACC	RCV000021796.1,