rs547339082

Orientation

plus

Stabilized

plus

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

Make rs547339082(C;T)

Make rs547339082(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

1503955

Gene

TPO

is a	snp
is	mentioned by
dbSNP	rs547339082
dbSNP (classic)	rs547339082
ClinGen	rs547339082
ebi	rs547339082
HLI	rs547339082
Exac	rs547339082
Gnomad	rs547339082
Varsome	rs547339082
LitVar	rs547339082
Map	rs547339082
PheGenI	rs547339082
Biobank	rs547339082
1000 genomes	rs547339082
hgdp	rs547339082
ensembl	rs547339082
geneview	rs547339082
scholar	rs547339082
google	rs547339082
pharmgkb	rs547339082
gwascentral	rs547339082
openSNP	rs547339082
23andMe	rs547339082
SNPshot	rs547339082
SNPdbe	rs547339082
MSV3d	rs547339082
GWAS Ctlg	rs547339082

Max Magnitude

0

ClinVar
Risk	rs547339082(T;T)
Alt	rs547339082(T;T)
Reference	Rs547339082(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TPO
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.1507727C>A
CLNSRC
CLNACC	RCV000494619.1,