rs377767406

Orientation

plus

Stabilized

plus

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

Make rs377767406(A;A)

Make rs377767406(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114491

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767406
dbSNP (classic)	rs377767406
ClinGen	rs377767406
ebi	rs377767406
HLI	rs377767406
Exac	rs377767406
Gnomad	rs377767406
Varsome	rs377767406
LitVar	rs377767406
Map	rs377767406
PheGenI	rs377767406
Biobank	rs377767406
1000 genomes	rs377767406
hgdp	rs377767406
ensembl	rs377767406
geneview	rs377767406
scholar	rs377767406
google	rs377767406
pharmgkb	rs377767406
gwascentral	rs377767406
openSNP	rs377767406
23andMe	rs377767406
SNPshot	rs377767406
SNPdbe	rs377767406
MSV3d	rs377767406
GWAS Ctlg	rs377767406

Max Magnitude

0

ClinVar
Risk	rs377767406(A;A) rs377767406(T;T)
Alt	rs377767406(A;A) rs377767406(T;T)
Reference	Rs377767406(G;G)
Significance	Pathogenic
Disease	MEN2 phenotype: Unknown Multiple endocrine neoplasia Hereditary cancer-predisposing syndrome
Variation	info
Gene	RET
CLNDBN	MEN2 phenotype: Unknown Multiple endocrine neoplasia, type 2a Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000010.10:g.43609939G>A; NC_000010.10:g.43609939G>T
CLNSRC	ClinVar
CLNACC	RCV000021811.1, RCV000021812.1, RCV000219970.1,