rs377767429

Orientation

plus

Stabilized

plus

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

Make rs377767429(GC;TT)

Make rs377767429(TT;TT)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43120120

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767429
dbSNP (classic)	rs377767429
ClinGen	rs377767429
ebi	rs377767429
HLI	rs377767429
Exac	rs377767429
Gnomad	rs377767429
Varsome	rs377767429
LitVar	rs377767429
Map	rs377767429
PheGenI	rs377767429
Biobank	rs377767429
1000 genomes	rs377767429
hgdp	rs377767429
ensembl	rs377767429
geneview	rs377767429
scholar	rs377767429
google	rs377767429
pharmgkb	rs377767429
gwascentral	rs377767429
openSNP	rs377767429
23andMe	rs377767429
SNPshot	rs377767429
SNPdbe	rs377767429
MSV3d	rs377767429
GWAS Ctlg	rs377767429

Max Magnitude

0

ClinVar
Risk	rs377767429(TT;TT)
Alt	rs377767429(TT;TT)
Reference	Rs377767429(GC;GC)
Significance	Other
Disease	Multiple endocrine neoplasia Medullary thyroid carcinoma Multiple endocrine neoplasia Multiple endocrine neoplasia Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2b Medullary thyroid carcinoma Multiple endocrine neoplasia, type 1 Multiple endocrine neoplasia, type 2a Multiple endocrine neoplasia, type 4
Reversed	0
HGVS	NC_000010.10:g.43615568_43615569delGCinsTT
CLNSRC	ClinVar
CLNACC	RCV000021873.1, RCV000422001.1, RCV000426500.1, RCV000433892.1, RCV000445104.1,