rs377767426

Orientation

plus

Stabilized

plus

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

Make rs377767426(C;G)

Make rs377767426(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43119694

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767426
dbSNP (classic)	rs377767426
ClinGen	rs377767426
ebi	rs377767426
HLI	rs377767426
Exac	rs377767426
Gnomad	rs377767426
Varsome	rs377767426
LitVar	rs377767426
Map	rs377767426
PheGenI	rs377767426
Biobank	rs377767426
1000 genomes	rs377767426
hgdp	rs377767426
ensembl	rs377767426
geneview	rs377767426
scholar	rs377767426
google	rs377767426
pharmgkb	rs377767426
gwascentral	rs377767426
openSNP	rs377767426
23andMe	rs377767426
SNPshot	rs377767426
SNPdbe	rs377767426
MSV3d	rs377767426
GWAS Ctlg	rs377767426

Max Magnitude

0

ClinVar
Risk	rs377767426(G;G)
Alt	rs377767426(G;G)
Reference	Rs377767426(C;C)
Significance	Pathogenic
Disease	Unclassifed Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	Unclassifed Multiple endocrine neoplasia, type 2
Reversed	0
HGVS	NC_000010.10:g.43615142C>G
CLNSRC	ClinVar
CLNACC	RCV000021869.1, RCV000204335.3,