rs794728684

Orientation

plus

Stabilized

plus

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

Make rs794728684(A;T)

Make rs794728684(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

43077259

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs794728684
dbSNP (classic)	rs794728684
ClinGen	rs794728684
ebi	rs794728684
HLI	rs794728684
Exac	rs794728684
Gnomad	rs794728684
Varsome	rs794728684
LitVar	rs794728684
Map	rs794728684
PheGenI	rs794728684
Biobank	rs794728684
1000 genomes	rs794728684
hgdp	rs794728684
ensembl	rs794728684
geneview	rs794728684
scholar	rs794728684
google	rs794728684
pharmgkb	rs794728684
gwascentral	rs794728684
openSNP	rs794728684
23andMe	rs794728684
SNPshot	rs794728684
SNPdbe	rs794728684
MSV3d	rs794728684
GWAS Ctlg	rs794728684

Max Magnitude

0

ClinVar
Risk	rs794728684(T;T)
Alt	rs794728684(T;T)
Reference	Rs794728684(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RET
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.43572707A>T
CLNSRC
CLNACC	RCV000182578.1,