rs377767409

Orientation

plus

Stabilized

plus

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

Make rs377767409(GC;TG)

Make rs377767409(TG;TG)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114501

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767409
dbSNP (classic)	rs377767409
ClinGen	rs377767409
ebi	rs377767409
HLI	rs377767409
Exac	rs377767409
Gnomad	rs377767409
Varsome	rs377767409
LitVar	rs377767409
Map	rs377767409
PheGenI	rs377767409
Biobank	rs377767409
1000 genomes	rs377767409
hgdp	rs377767409
ensembl	rs377767409
geneview	rs377767409
scholar	rs377767409
google	rs377767409
pharmgkb	rs377767409
gwascentral	rs377767409
openSNP	rs377767409
23andMe	rs377767409
SNPshot	rs377767409
SNPdbe	rs377767409
MSV3d	rs377767409
GWAS Ctlg	rs377767409

Max Magnitude

0

ClinVar
Risk	rs377767409(TG;TG)
Alt	rs377767409(TG;TG)
Reference	Rs377767409(GC;GC)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2a
Reversed	0
HGVS	NC_000010.10:g.43609949_43609950delGCinsTG
CLNSRC	ClinVar
CLNACC	RCV000021826.1,