rs377767398

Orientation

plus

Stabilized

plus

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

Make rs377767398(AT;AT)

Make rs377767398(AT;GC)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43113628

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767398
dbSNP (classic)	rs377767398
ClinGen	rs377767398
ebi	rs377767398
HLI	rs377767398
Exac	rs377767398
Gnomad	rs377767398
Varsome	rs377767398
LitVar	rs377767398
Map	rs377767398
PheGenI	rs377767398
Biobank	rs377767398
1000 genomes	rs377767398
hgdp	rs377767398
ensembl	rs377767398
geneview	rs377767398
scholar	rs377767398
google	rs377767398
pharmgkb	rs377767398
gwascentral	rs377767398
openSNP	rs377767398
23andMe	rs377767398
SNPshot	rs377767398
SNPdbe	rs377767398
MSV3d	rs377767398
GWAS Ctlg	rs377767398

Max Magnitude

0

ClinVar
Risk	rs377767398(AT;AT) rs377767398(CT;CT) rs377767398(TT;TT)
Alt	rs377767398(AT;AT) rs377767398(CT;CT) rs377767398(TT;TT)
Reference	Rs377767398(GC;GC)
Significance	Pathogenic
Disease	MEN2 phenotype: Unclassified
Variation	info
Gene	RET
CLNDBN	MEN2 phenotype: Unclassified
Reversed	0
HGVS	NC_000010.10:g.43609076_43609077delGCinsAT; NC_000010.10:g.43609076_43609077delGCinsCT; NC_000010.10:g.43609076_43609077delGCinsTT
CLNSRC	ClinVar
CLNACC	RCV000021785.1, RCV000032028.1, RCV000032029.1,