rs377767389

Orientation

plus

Stabilized

plus

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

Make rs377767389(CT;CT)

Make rs377767389(CT;GC)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43112120

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767389
dbSNP (classic)	rs377767389
ClinGen	rs377767389
ebi	rs377767389
HLI	rs377767389
Exac	rs377767389
Gnomad	rs377767389
Varsome	rs377767389
LitVar	rs377767389
Map	rs377767389
PheGenI	rs377767389
Biobank	rs377767389
1000 genomes	rs377767389
hgdp	rs377767389
ensembl	rs377767389
geneview	rs377767389
scholar	rs377767389
google	rs377767389
pharmgkb	rs377767389
gwascentral	rs377767389
openSNP	rs377767389
23andMe	rs377767389
SNPshot	rs377767389
SNPdbe	rs377767389
MSV3d	rs377767389
GWAS Ctlg	rs377767389

Max Magnitude

0

ClinVar
Risk	rs377767389(CT;CT)
Alt	rs377767389(CT;CT)
Reference	Rs377767389(GC;GC)
Significance	Pathogenic
Disease	MEN2 phenotype: Unclassified
Variation	info
Gene	RET
CLNDBN	MEN2 phenotype: Unclassified
Reversed	0
HGVS	NC_000010.10:g.43607568_43607569delGCinsCT
CLNSRC	ClinVar
CLNACC	RCV000021765.1,