rs377767405

Orientation

plus

Stabilized

plus

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

Make rs377767405(A;A)

Make rs377767405(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43114489

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs377767405
dbSNP (classic)	rs377767405
ClinGen	rs377767405
ebi	rs377767405
HLI	rs377767405
Exac	rs377767405
Gnomad	rs377767405
Varsome	rs377767405
LitVar	rs377767405
Map	rs377767405
PheGenI	rs377767405
Biobank	rs377767405
1000 genomes	rs377767405
hgdp	rs377767405
ensembl	rs377767405
geneview	rs377767405
scholar	rs377767405
google	rs377767405
pharmgkb	rs377767405
gwascentral	rs377767405
openSNP	rs377767405
23andMe	rs377767405
SNPshot	rs377767405
SNPdbe	rs377767405
MSV3d	rs377767405
GWAS Ctlg	rs377767405

Max Magnitude

0

ClinVar
Risk	rs377767405(A;A) rs377767405(C;C) rs377767405(T;T)
Alt	rs377767405(A;A) rs377767405(C;C) rs377767405(T;T)
Reference	Rs377767405(G;G)
Significance	Pathogenic
Disease	MEN2A and Unclassified MEN2 phenotype: Unknown FMTC and Unclassified
Variation	info
Gene	RET
CLNDBN	MEN2A and Unclassified MEN2 phenotype: Unknown FMTC and Unclassified
Reversed	0
HGVS	NC_000010.10:g.43609937G>A; NC_000010.10:g.43609937G>C; NC_000010.10:g.43609937G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000021807.1, RCV000021808.1, RCV000021809.1,