rs1060500759

Orientation

plus

Stabilized

plus

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

Make rs1060500759(C;T)

Make rs1060500759(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

43120162

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs1060500759
dbSNP (classic)	rs1060500759
ClinGen	rs1060500759
ebi	rs1060500759
HLI	rs1060500759
Exac	rs1060500759
Gnomad	rs1060500759
Varsome	rs1060500759
LitVar	rs1060500759
Map	rs1060500759
PheGenI	rs1060500759
Biobank	rs1060500759
1000 genomes	rs1060500759
hgdp	rs1060500759
ensembl	rs1060500759
geneview	rs1060500759
scholar	rs1060500759
google	rs1060500759
pharmgkb	rs1060500759
gwascentral	rs1060500759
openSNP	rs1060500759
23andMe	rs1060500759
SNPshot	rs1060500759
SNPdbe	rs1060500759
MSV3d	rs1060500759
GWAS Ctlg	rs1060500759

Max Magnitude

0

ClinVar
Risk	rs1060500759(T;T)
Alt	rs1060500759(T;T)
Reference	Rs1060500759(C;C)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	RET
CLNDBN	Multiple endocrine neoplasia, type 2
Reversed	0
HGVS	NC_000010.10:g.43615610C>T
CLNSRC
CLNACC	RCV000461915.1,