rs377767422

Orientation

plus

Stabilized

plus

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

Make rs377767422(C;T)

Make rs377767422(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

43119635

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767422
dbSNP (classic)	rs377767422
ClinGen	rs377767422
ebi	rs377767422
HLI	rs377767422
Exac	rs377767422
Gnomad	rs377767422
Varsome	rs377767422
LitVar	rs377767422
Map	rs377767422
PheGenI	rs377767422
Biobank	rs377767422
1000 genomes	rs377767422
hgdp	rs377767422
ensembl	rs377767422
geneview	rs377767422
scholar	rs377767422
google	rs377767422
pharmgkb	rs377767422
gwascentral	rs377767422
openSNP	rs377767422
23andMe	rs377767422
SNPshot	rs377767422
SNPdbe	rs377767422
MSV3d	rs377767422
GWAS Ctlg	rs377767422

Max Magnitude

0

ClinVar
Risk	rs377767422(T;T)
Alt	rs377767422(T;T)
Reference	Rs377767422(C;C)
Significance	Probable-Pathogenic
Disease	MEN2 phenotype: Unknown not provided
Variation	info
Gene	RET
CLNDBN	MEN2 phenotype: Unknown not provided
Reversed	0
HGVS	NC_000010.10:g.43615083C>T
CLNSRC
CLNACC	RCV000021859.1, RCV000478761.1,