rs794728689

Orientation

plus

Stabilized

plus

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

Make rs794728689(-;-)

Make rs794728689(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

43123715

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs794728689
dbSNP (classic)	rs794728689
ClinGen	rs794728689
ebi	rs794728689
HLI	rs794728689
Exac	rs794728689
Gnomad	rs794728689
Varsome	rs794728689
LitVar	rs794728689
Map	rs794728689
PheGenI	rs794728689
Biobank	rs794728689
1000 genomes	rs794728689
hgdp	rs794728689
ensembl	rs794728689
geneview	rs794728689
scholar	rs794728689
google	rs794728689
pharmgkb	rs794728689
gwascentral	rs794728689
openSNP	rs794728689
23andMe	rs794728689
SNPshot	rs794728689
SNPdbe	rs794728689
MSV3d	rs794728689
GWAS Ctlg	rs794728689

Max Magnitude

0

ClinVar
Risk	rs794728689(-;-)
Alt	rs794728689(-;-)
Reference	Rs794728689(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RET
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.43619163delG
CLNSRC
CLNACC	RCV000182592.2,