rs377767416

Orientation

plus

Stabilized

plus

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

Make rs377767416(A;G)

Make rs377767416(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43118430

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767416
dbSNP (classic)	rs377767416
ClinGen	rs377767416
ebi	rs377767416
HLI	rs377767416
Exac	rs377767416
Gnomad	rs377767416
Varsome	rs377767416
LitVar	rs377767416
Map	rs377767416
PheGenI	rs377767416
Biobank	rs377767416
1000 genomes	rs377767416
hgdp	rs377767416
ensembl	rs377767416
geneview	rs377767416
scholar	rs377767416
google	rs377767416
pharmgkb	rs377767416
gwascentral	rs377767416
openSNP	rs377767416
23andMe	rs377767416
SNPshot	rs377767416
SNPdbe	rs377767416
MSV3d	rs377767416
GWAS Ctlg	rs377767416

Max Magnitude

0

ClinVar
Risk	rs377767416(G;G)
Alt	rs377767416(G;G)
Reference	Rs377767416(A;A)
Significance	Pathogenic
Disease	MEN2 phenotype: Unclassified Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	MEN2 phenotype: Unclassified Multiple endocrine neoplasia, type 2
Reversed	0
HGVS	NC_000010.10:g.43613878A>G
CLNSRC	ClinVar
CLNACC	RCV000021848.1, RCV000232536.1,