rs377767391

Orientation

plus

Stabilized

plus

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

Make rs377767391(A;A)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43113627

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767391
dbSNP (classic)	rs377767391
ClinGen	rs377767391
ebi	rs377767391
HLI	rs377767391
Exac	rs377767391
Gnomad	rs377767391
Varsome	rs377767391
LitVar	rs377767391
Map	rs377767391
PheGenI	rs377767391
Biobank	rs377767391
1000 genomes	rs377767391
hgdp	rs377767391
ensembl	rs377767391
geneview	rs377767391
scholar	rs377767391
google	rs377767391
pharmgkb	rs377767391
gwascentral	rs377767391
openSNP	rs377767391
23andMe	rs377767391
SNPshot	rs377767391
SNPdbe	rs377767391
MSV3d	rs377767391
GWAS Ctlg	rs377767391

Max Magnitude

5.1

ClinVar
Risk	rs377767391(A;A) rs377767391(C;C) rs377767391(G;G)
Alt	rs377767391(A;A) rs377767391(C;C) rs377767391(G;G)
Reference	Rs377767391(T;T)
Significance	Pathogenic
Disease	MEN2 phenotype: Unclassified FMTC and Unclassified
Variation	info
Gene	RET
CLNDBN	MEN2 phenotype: Unclassified FMTC and Unclassified
Reversed	0
HGVS	NC_000010.10:g.43609075T>A; NC_000010.10:g.43609075T>C; NC_000010.10:g.43609075T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000021769.1, RCV000021782.1, RCV000021783.1,