rs794728685

Orientation

plus

Stabilized

plus

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

Make rs794728685(A;G)

Make rs794728685(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

43119680

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs794728685
dbSNP (classic)	rs794728685
ClinGen	rs794728685
ebi	rs794728685
HLI	rs794728685
Exac	rs794728685
Gnomad	rs794728685
Varsome	rs794728685
LitVar	rs794728685
Map	rs794728685
PheGenI	rs794728685
Biobank	rs794728685
1000 genomes	rs794728685
hgdp	rs794728685
ensembl	rs794728685
geneview	rs794728685
scholar	rs794728685
google	rs794728685
pharmgkb	rs794728685
gwascentral	rs794728685
openSNP	rs794728685
23andMe	rs794728685
SNPshot	rs794728685
SNPdbe	rs794728685
MSV3d	rs794728685
GWAS Ctlg	rs794728685

Max Magnitude

0

ClinVar
Risk	rs794728685(G;G)
Alt	rs794728685(G;G)
Reference	Rs794728685(A;A)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	RET
CLNDBN	not specified
Reversed	0
HGVS	NC_000010.10:g.43615128A>G
CLNSRC
CLNACC	RCV000182586.2,