rs377767396

Orientation

plus

Stabilized

plus

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

Make rs377767396(C;G)

Make rs377767396(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43113623

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767396
dbSNP (classic)	rs377767396
ClinGen	rs377767396
ebi	rs377767396
HLI	rs377767396
Exac	rs377767396
Gnomad	rs377767396
Varsome	rs377767396
LitVar	rs377767396
Map	rs377767396
PheGenI	rs377767396
Biobank	rs377767396
1000 genomes	rs377767396
hgdp	rs377767396
ensembl	rs377767396
geneview	rs377767396
scholar	rs377767396
google	rs377767396
pharmgkb	rs377767396
gwascentral	rs377767396
openSNP	rs377767396
23andMe	rs377767396
SNPshot	rs377767396
SNPdbe	rs377767396
MSV3d	rs377767396
GWAS Ctlg	rs377767396

Max Magnitude

0

ClinVar
Risk	rs377767396(G;G)
Alt	rs377767396(G;G)
Reference	Rs377767396(C;C)
Significance	Probable-Pathogenic
Disease	No MEN2 disease
Variation	info
Gene	RET
CLNDBN	No MEN2 disease
Reversed	0
HGVS	NC_000010.10:g.43609071C>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000021781.1,