rs377767437

Orientation

plus

Stabilized

plus

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

Make rs377767437(TGCCGCACG;TGCCGCACG)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114508

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767437
dbSNP (classic)	rs377767437
ClinGen	rs377767437
ebi	rs377767437
HLI	rs377767437
Exac	rs377767437
Gnomad	rs377767437
Varsome	rs377767437
LitVar	rs377767437
Map	rs377767437
PheGenI	rs377767437
Biobank	rs377767437
1000 genomes	rs377767437
hgdp	rs377767437
ensembl	rs377767437
geneview	rs377767437
scholar	rs377767437
google	rs377767437
pharmgkb	rs377767437
gwascentral	rs377767437
openSNP	rs377767437
23andMe	rs377767437
SNPshot	rs377767437
SNPdbe	rs377767437
MSV3d	rs377767437
GWAS Ctlg	rs377767437

Max Magnitude

5.1

ClinVar
Risk	rs377767437(GTGCCGCAC;GTGCCGCAC)
Alt	rs377767437(GTGCCGCAC;GTGCCGCAC)
Reference	Rs377767437(-;-)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2a
Reversed	0
HGVS	NC_000010.10:g.43609948_43609956dupTGCCGCACG
CLNSRC	ClinVar
CLNACC	RCV000021831.1,