rs377767438

Orientation

plus

Stabilized

plus

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

Make rs377767438(A;GACCTGTGCCGCC)

Make rs377767438(GACCTGTGCCGCC;GACCTGTGCCGCC)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114506

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767438
dbSNP (classic)	rs377767438
ClinGen	rs377767438
ebi	rs377767438
HLI	rs377767438
Exac	rs377767438
Gnomad	rs377767438
Varsome	rs377767438
LitVar	rs377767438
Map	rs377767438
PheGenI	rs377767438
Biobank	rs377767438
1000 genomes	rs377767438
hgdp	rs377767438
ensembl	rs377767438
geneview	rs377767438
scholar	rs377767438
google	rs377767438
pharmgkb	rs377767438
gwascentral	rs377767438
openSNP	rs377767438
23andMe	rs377767438
SNPshot	rs377767438
SNPdbe	rs377767438
MSV3d	rs377767438
GWAS Ctlg	rs377767438

Max Magnitude

0

ClinVar
Risk	rs377767438(GACCTGTGCCGCC;GACCTGTGCCGCC)
Alt	rs377767438(GACCTGTGCCGCC;GACCTGTGCCGCC)
Reference	Rs377767438(A;A)
Significance	Pathogenic
Disease	MEN2 phenotype: Unclassified
Variation	info
Gene	RET
CLNDBN	MEN2 phenotype: Unclassified
Reversed	0
HGVS	NC_000010.10:g.43609954delAinsGACCTGTGCCGCC
CLNSRC	ClinVar
CLNACC	RCV000021830.1,