rs377767436

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;ACGAGCTGTGCC)	5.1	Multiple Endocrine Neoplasia IIA

Make rs377767436(ACGAGCTGTGCC;ACGAGCTGTGCC)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114503

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767436
dbSNP (classic)	rs377767436
ClinGen	rs377767436
ebi	rs377767436
HLI	rs377767436
Exac	rs377767436
Gnomad	rs377767436
Varsome	rs377767436
LitVar	rs377767436
Map	rs377767436
PheGenI	rs377767436
Biobank	rs377767436
1000 genomes	rs377767436
hgdp	rs377767436
ensembl	rs377767436
geneview	rs377767436
scholar	rs377767436
google	rs377767436
pharmgkb	rs377767436
gwascentral	rs377767436
openSNP	rs377767436
23andMe	rs377767436
SNPshot	rs377767436
SNPdbe	rs377767436
MSV3d	rs377767436
GWAS Ctlg	rs377767436

Max Magnitude

5.1

ClinVar
Risk	rs377767436(ACGAGCTGTGCC;ACGAGCTGTGCC)
Alt	rs377767436(ACGAGCTGTGCC;ACGAGCTGTGCC)
Reference	Rs377767436(-;-)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2a
Reversed	0
HGVS	NC_000010.10:g.43609940_43609951dupACGAGCTGTGCC
CLNSRC	ClinVar
CLNACC	RCV000021829.1,