rs377767428

Orientation

plus

Stabilized

plus

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

Make rs377767428(A;A)

Make rs377767428(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43120120

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767428
dbSNP (classic)	rs377767428
ClinGen	rs377767428
ebi	rs377767428
HLI	rs377767428
Exac	rs377767428
Gnomad	rs377767428
Varsome	rs377767428
LitVar	rs377767428
Map	rs377767428
PheGenI	rs377767428
Biobank	rs377767428
1000 genomes	rs377767428
hgdp	rs377767428
ensembl	rs377767428
geneview	rs377767428
scholar	rs377767428
google	rs377767428
pharmgkb	rs377767428
gwascentral	rs377767428
openSNP	rs377767428
23andMe	rs377767428
SNPshot	rs377767428
SNPdbe	rs377767428
MSV3d	rs377767428
GWAS Ctlg	rs377767428

Max Magnitude

0

ClinVar
Risk	rs377767428(A;A)
Alt	rs377767428(A;A)
Reference	Rs377767428(G;G)
Significance	Pathogenic
Disease	MEN2 phenotype: Unclassified
Variation	info
Gene	RET
CLNDBN	MEN2 phenotype: Unclassified
Reversed	0
HGVS	NC_000010.10:g.43615568G>A
CLNSRC	ClinVar
CLNACC	RCV000021872.1,