rs143862573

Orientation

plus

Stabilized

plus

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

Make rs143862573(A;A)

Make rs143862573(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

43119750

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs143862573
dbSNP (classic)	rs143862573
ClinGen	rs143862573
ebi	rs143862573
HLI	rs143862573
Exac	rs143862573
Gnomad	rs143862573
Varsome	rs143862573
LitVar	rs143862573
Map	rs143862573
PheGenI	rs143862573
Biobank	rs143862573
1000 genomes	rs143862573
hgdp	rs143862573
ensembl	rs143862573
geneview	rs143862573
scholar	rs143862573
google	rs143862573
pharmgkb	rs143862573
gwascentral	rs143862573
openSNP	rs143862573
23andMe	rs143862573
SNPshot	rs143862573
SNPdbe	rs143862573
MSV3d	rs143862573
GWAS Ctlg	rs143862573

Max Magnitude

0

ClinVar
Risk	rs143862573(A;A) rs143862573(T;T)
Alt	rs143862573(A;A) rs143862573(T;T)
Reference	Rs143862573(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RET
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.43615198G>A
CLNSRC
CLNACC	RCV000413101.1,